Source: ALL
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: rs121907947
rs121907947
SERPING1
2 0.925 0.160 11 57614450 missense variant G/A snv 0.700 0
dbSNP: rs121907948
rs121907948
SERPING1
3 0.882 0.160 11 57614475 missense variant G/A;C;T snv 0.700 0
dbSNP: rs121907949
rs121907949
SERPING1
2 0.925 0.160 11 57614439 missense variant T/A snv 0.700 0
dbSNP: rs28940870
rs28940870
SERPING1
3 0.882 0.160 11 57614474 missense variant C/A;T snv 0.700 0
dbSNP: rs606231141
rs606231141
SERPING1
1 1.000 0.160 11 57614435 protein altering variant -/TGT ins 0.700 0