Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs35974739
rs35974739
1.000 0.080 16 177376 missense variant T/C snv
CUI: C0272006
Disease: Unstable hemoglobin disease
Unstable hemoglobin disease
0.010 1.000 1 1993 1993
dbSNP: rs63751417
rs63751417
1.000 0.080 16 173565 missense variant T/C snv
CUI: C0272006
Disease: Unstable hemoglobin disease
Unstable hemoglobin disease
0.010 1.000 1 1993 1993