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: rs61902492
rs61902492
1 11 113121199 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7938812
rs7938812
1 11 113040282 intron variant T/A;G snv 0.700 1.000 1 2019 2019