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: rs752997229
rs752997229
1 1.000 0.080 17 1650882 missense variant T/C;G snv 4.0E-06 1.4E-05 0.700 1.000 1 2001 2001
dbSNP: rs1555550617
rs1555550617
2 0.925 0.080 17 1655533 missense variant C/T snv 0.700 0