SCMH1, Scm polycomb group protein homolog 1, 22955

N. diseases: 11; N. variants: 11
Disease: Atrial Fibrillation ×
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: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2018 2018