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rs10423674

From SNPedia

Orientationplus
Stabilizedplus
Make rs10423674(A;A)
Make rs10423674(A;C)
Make rs10423674(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position18707093
GeneCRTC1
is asnp
is mentioned by
dbSNPrs10423674
ebirs10423674
HLIrs10423674
Exacrs10423674
Varsomers10423674
Maprs10423674
PheGenIrs10423674
hapmaprs10423674
1000 genomesrs10423674
hgdprs10423674
ensemblrs10423674
gopubmedrs10423674
geneviewrs10423674
scholarrs10423674
googlers10423674
pharmgkbrs10423674
gwascentralrs10423674
openSNPrs10423674
23andMers10423674
23andMe allrs10423674
SNP Nexus

SNPshotrs10423674
SNPdbers10423674
MSV3drs10423674
GWAS Ctlgrs10423674
GMAF0.4972
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21102462OA-icon.png]
Trait
Title Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Risk Allele A
P-val 6E-9
Odds Ratio 2.3000 [1.52-3.08] week decrease


[PMID 25447851OA-icon.png] Polymorphisms Near TBX5 and GDF7 are Associated with Increased Risk for Barrett's Esophagus