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: rs33927093
rs33927093
HBB
1 1.000 0.040 11 5225620 missense variant G/A;T snv 0.010 1.000 1 1995 1995
dbSNP: rs35594230
rs35594230
HBB
1 1.000 0.040 11 5225626 missense variant G/A snv 0.010 1.000 1 1995 1995