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: rs10249651
rs10249651
1 1.000 0.040 7 117424571 intron variant T/C snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs975722
rs975722
1 1.000 0.040 7 117692860 intron variant A/G snv 0.53 0.700 1.000 1 2018 2018