SCMH1, Scm polycomb group protein homolog 1, 22955

N. diseases: 11; N. variants: 11
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2885697
rs2885697
1.000 0.080 1 41078607 intron variant G/T snv 0.72
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2019 2019