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: rs886041081
rs886041081
4 0.925 4 185144891 missense variant G/A snv 0.700 0
dbSNP: rs886041082
rs886041082
2 1.000 4 185145863 missense variant C/G snv 0.700 0