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: rs1558079436
rs1558079436
3 0.925 0.040 1 162773569 missense variant T/C snv 0.700 0
dbSNP: rs1558081627
rs1558081627
2 1.000 0.040 1 162776306 missense variant A/G snv 0.700 0