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: rs1295540039
rs1295540039
SLC4A7
1 1.000 0.160 3 27390094 missense variant C/T snv 8.2E-06 1.4E-05 0.010 1.000 1 2017 2017