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rs13037749

From SNPedia

Orientationplus
Stabilizedplus
Make rs13037749(A;A)
Make rs13037749(A;G)
Make rs13037749(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position41435919
GeneCHD6
is asnp
is mentioned by
dbSNPrs13037749
ebirs13037749
HLIrs13037749
Exacrs13037749
Varsomers13037749
Maprs13037749
PheGenIrs13037749
hapmaprs13037749
1000 genomesrs13037749
hgdprs13037749
ensemblrs13037749
gopubmedrs13037749
geneviewrs13037749
scholarrs13037749
googlers13037749
pharmgkbrs13037749
gwascentralrs13037749
openSNPrs13037749
23andMers13037749
23andMe allrs13037749
SNP Nexus

SNPshotrs13037749
SNPdbers13037749
MSV3drs13037749
GWAS Ctlgrs13037749
GMAF0.02893
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele A
P-val 0.000008
Odds Ratio None None