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: rs3278
rs3278
SLC4A7
1 1.000 0.080 3 27433860 intron variant G/A snv 0.13 0.010 1.000 1 2007 2007