At http://www.ianlogan.co.uk/23andme/23andMe_index2.htm someone has made a lovely program that goes through your results and shows the ones which have rare alleles (present in less than 1% of the population).
While rarities are not necessarily indicative of a resulting dysfunction, they do present a nice place to start looking at things. Anyhow, maybe we can post our rare results here and compare to see if there's any trends?
I've got 53 SNPs with rare alleles, two of which are homozygous. But one of those is apparently due to a mistake from 23andMe, so I'm really just homozygous for rs17526980 on the KIF13B gene. MA = Minor Alleles, and ones resulting in a missense or similar mutation are orange. My homozygous result is red. VAL = Valentijn's genotype.
RSID.......GENE........MA..VAL
rs12202093..??..........C..CT
rs313273....??..........A..AG
rs12845411..??..........T..CT
rs11765511..??..........T..CT
rs1364778...??..........A..AG
rs2448326...??..........T..GT
rs10036862..??..........A..AG
rs1407268...??..........G..AG
rs12154319..ABCB1.......A..AG
rs56131651..ABCC2.......A..AG
rs3730044...ACE.........A..AG
rs7713754...AFF4........C..CT
rs11239373..ANKRD30BP3..C..CT
rs11246353..AP2A2.......A..AG
rs41273157..ATP13A2.....T..CT
rs11797182..BEX1........G..AG
rs17394875..CACHD1......T..CT
rs3848286...CES2........A..AG
rs8176928...DNASE1......G..GG
rs12534498..DTX2........A..AG
rs2332284...PARP9.......C..CT
rs5894......F2R.........G..GT
rs9332688...F5..........A..AG
rs428199....F9..........T..CT
rs11239604..FAM21C......G..AG
rs12194562..GRM1........C..CT
rs62638620..GRM6........A..AG
rs306781....GSN.........C..CT
rs3218808...GTF2H4......T..CT
rs3218816...GTF2H4......A..AG
rs2857533...HOXD3.......T..GT
rs1805128...KCNE1.......T..CT
rs17526980..KIF13B......T..TT
rs3212379...MC1R........T..CT
rs1611772...MUC1........A..AG
rs1799931...NAT2........A..AG
rs4648039...NFKB1.......T..CT
rs35722504..PARN........T..CT
rs725522....PCSK1.......A..AG
rs12195007..PHACTR1.....G..GT
rs4135292...PPARG.......A..AG
rs17219643..PTPRT.......T..CT
rs36074402..RAB38.......A..AG
rs10935780..RNF13.......C..CT
rs36049418..SLC12A3.....A..AG
rs2328894...SLC17A4.....T..CT
rs724665....SLC25A40....A..AG
rs28914833..SLC6A4......G..AG
rs9860312...STAC........T..CT
rs4361233...SUSD5.......G..AG
rs526433....TECTA.......G..AG
rs12884433..TSHR........T..CT
rs11011379..ZNF248......C..CT
While rarities are not necessarily indicative of a resulting dysfunction, they do present a nice place to start looking at things. Anyhow, maybe we can post our rare results here and compare to see if there's any trends?
I've got 53 SNPs with rare alleles, two of which are homozygous. But one of those is apparently due to a mistake from 23andMe, so I'm really just homozygous for rs17526980 on the KIF13B gene. MA = Minor Alleles, and ones resulting in a missense or similar mutation are orange. My homozygous result is red. VAL = Valentijn's genotype.
RSID.......GENE........MA..VAL
rs12202093..??..........C..CT
rs313273....??..........A..AG
rs12845411..??..........T..CT
rs11765511..??..........T..CT
rs1364778...??..........A..AG
rs2448326...??..........T..GT
rs10036862..??..........A..AG
rs1407268...??..........G..AG
rs12154319..ABCB1.......A..AG
rs56131651..ABCC2.......A..AG
rs3730044...ACE.........A..AG
rs7713754...AFF4........C..CT
rs11239373..ANKRD30BP3..C..CT
rs11246353..AP2A2.......A..AG
rs41273157..ATP13A2.....T..CT
rs11797182..BEX1........G..AG
rs17394875..CACHD1......T..CT
rs3848286...CES2........A..AG
rs12534498..DTX2........A..AG
rs2332284...PARP9.......C..CT
rs5894......F2R.........G..GT
rs9332688...F5..........A..AG
rs428199....F9..........T..CT
rs11239604..FAM21C......G..AG
rs12194562..GRM1........C..CT
rs62638620..GRM6........A..AG
rs306781....GSN.........C..CT
rs3218808...GTF2H4......T..CT
rs3218816...GTF2H4......A..AG
rs2857533...HOXD3.......T..GT
rs1805128...KCNE1.......T..CT
rs17526980..KIF13B......T..TT
rs3212379...MC1R........T..CT
rs1611772...MUC1........A..AG
rs1799931...NAT2........A..AG
rs4648039...NFKB1.......T..CT
rs35722504..PARN........T..CT
rs725522....PCSK1.......A..AG
rs12195007..PHACTR1.....G..GT
rs4135292...PPARG.......A..AG
rs17219643..PTPRT.......T..CT
rs36074402..RAB38.......A..AG
rs10935780..RNF13.......C..CT
rs36049418..SLC12A3.....A..AG
rs2328894...SLC17A4.....T..CT
rs724665....SLC25A40....A..AG
rs28914833..SLC6A4......G..AG
rs9860312...STAC........T..CT
rs4361233...SUSD5.......G..AG
rs526433....TECTA.......G..AG
rs12884433..TSHR........T..CT
rs11011379..ZNF248......C..CT