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rs6954796

From SNPedia

Orientationplus
Stabilizedplus
Make rs6954796(C;C)
Make rs6954796(C;G)
Make rs6954796(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position20047359
GeneAC005062.2
is asnp
is mentioned by
dbSNPrs6954796
ebirs6954796
HLIrs6954796
Exacrs6954796
Varsomers6954796
Maprs6954796
PheGenIrs6954796
hapmaprs6954796
1000 genomesrs6954796
hgdprs6954796
ensemblrs6954796
gopubmedrs6954796
geneviewrs6954796
scholarrs6954796
googlers6954796
pharmgkbrs6954796
gwascentralrs6954796
openSNPrs6954796
23andMers6954796
23andMe allrs6954796
SNP Nexus

SNPshotrs6954796
SNPdbers6954796
MSV3drs6954796
GWAS Ctlgrs6954796
GMAF0.2066
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23738518OA-icon.png]
Trait Non-word repetition
Title A genome-wide association study for reading and language abilities in two population cohorts.
Risk Allele C
P-val 2E-6
Odds Ratio .12 [0.073-0.175] unit increase