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: rs121912585
rs121912585
4 0.851 0.160 12 39332405 missense variant G/A snv 0.700 0
dbSNP: rs121912586
rs121912586
3 0.882 0.160 12 39332404 missense variant C/T snv 0.700 0
dbSNP: rs267607200
rs267607200
1 1.000 0.160 12 39332606 missense variant C/T snv 0.700 0