Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137853036
rs137853036
0.923 0.036 2 46380281 missense variant G/A,T snp
CUI: C2673187
Disease: Erythrocytosis, Familial, 4
Erythrocytosis, Familial, 4
Hemic and Lymphatic Diseases 0.800 3 2008 2009
dbSNP: rs137853037
rs137853037
1.000 0.036 2 46380275 missense variant A/G snp
CUI: C2673187
Disease: Erythrocytosis, Familial, 4
Erythrocytosis, Familial, 4
Hemic and Lymphatic Diseases 0.800 2 2008 2009