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: rs72549407
rs72549407
FAM126A
1 1.000 0.160 7 22978444 missense variant A/C;G snv 2.0E-05 0.800 1.000 4 2006 2016