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: rs698078
rs698078
1 3 186741438 intron variant A/G snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs710446
rs710446
4 0.925 0.120 3 186742138 missense variant T/C snv 0.42 0.44 0.010 1.000 1 2015 2015