SCMH1, Scm polycomb group protein homolog 1, 22955

N. diseases: 11; N. variants: 11
Disease: mathematical ability ×
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: rs12024115
rs12024115 		1 41068685 intron variant C/T snv 0.11
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2284801
rs2284801 		1 41158056 intron variant G/C snv 0.18
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018