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: rs162509
rs162509
3 0.925 0.160 21 26953456 intron variant C/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs226794
rs226794
3 0.882 0.160 21 26930036 missense variant A/G snv 0.83 0.89 0.010 1.000 1 2017 2017