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rs2239774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2239774(C;C)
Make rs2239774(C;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37241613
GeneRAC2
is asnp
is mentioned by
dbSNPrs2239774
ebirs2239774
HLIrs2239774
Exacrs2239774
Varsomers2239774
Maprs2239774
PheGenIrs2239774
hapmaprs2239774
1000 genomesrs2239774
hgdprs2239774
ensemblrs2239774
gopubmedrs2239774
geneviewrs2239774
scholarrs2239774
googlers2239774
pharmgkbrs2239774
gwascentralrs2239774
openSNPrs2239774
23andMers2239774
23andMe allrs2239774
SNP Nexus

SNPshotrs2239774
SNPdbers2239774
MSV3drs2239774
GWAS Ctlgrs2239774
GMAF0.169
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 19505917OA-icon.png] Lead exposure, polymorphisms in genes related to oxidative stress, and risk of adult brain tumors


ClinVar
Risk rs2239774(C;C)
Alt rs2239774(C;C)
Reference rs2239774(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene RAC2
CLNDBN not specified
Reversed 0
HGVS NC_000022.10:g.37637653G>C
CLNSRC ClinVar GeneDx
CLNACC RCV000127684.1,