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: rs3761472
rs3761472
SAMM50
2 0.925 0.040 22 43972242 missense variant A/G snv 0.21 0.18 0.710 1.000 2 2013 2018