Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1531343
rs1531343
2 0.925 0.160 12 65781114 intron variant G/C;T snv 0.810 1.000 5 2010 2017
dbSNP: rs2261181
rs2261181
1 1.000 0.080 12 65818538 intron variant C/T snv 0.13 0.800 1.000 4 2012 2018
dbSNP: rs2258238
rs2258238
1 1.000 0.080 12 65827280 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2612035
rs2612035
1 1.000 0.080 12 65798887 intron variant A/G;T snv 0.700 1.000 1 2012 2012