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: rs111033258
rs111033258
7 0.851 0.200 3 150972565 missense variant A/C snv 2.7E-04 1.5E-04 0.700 0
dbSNP: rs121908143
rs121908143
6 0.827 0.200 3 150972591 missense variant A/C;G snv 8.0E-05; 4.0E-06 0.700 0