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rs130067

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs130067(A;C)
Make rs130067(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31150734
GeneCCHCR1
is asnp
is mentioned by
dbSNPrs130067
ebirs130067
HLIrs130067
Exacrs130067
Varsomers130067
Maprs130067
PheGenIrs130067
hapmaprs130067
1000 genomesrs130067
hgdprs130067
ensemblrs130067
gopubmedrs130067
geneviewrs130067
scholarrs130067
googlers130067
pharmgkbrs130067
gwascentralrs130067
openSNPrs130067
23andMers130067
23andMe allrs130067
SNP Nexus

SNPshotrs130067
SNPdbers130067
MSV3drs130067
GWAS Ctlgrs130067
GMAF0.2447
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21743467OA-icon.png]
Trait
Title Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.
Risk Allele G
P-val 3E-8
Odds Ratio 1.0500 [1.02-1.09]


GET Evidence
CCHCR1-E364D
aa_change Glu364Asp
aa_change_short E364D
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.195242
summary



[PMID 22985493OA-icon.png] Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis.