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rs726640

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs726640(C;T)
Make rs726640(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159685728
is asnp
is mentioned by
dbSNPrs726640
ebirs726640
HLIrs726640
Exacrs726640
Varsomers726640
Maprs726640
PheGenIrs726640
hapmaprs726640
1000 genomesrs726640
hgdprs726640
ensemblrs726640
gopubmedrs726640
geneviewrs726640
scholarrs726640
googlers726640
pharmgkbrs726640
gwascentralrs726640
openSNPrs726640
23andMers726640
23andMe allrs726640
SNP Nexus

SNPshotrs726640
SNPdbers726640
MSV3drs726640
GWAS Ctlgrs726640
GMAF0.03719
Max Magnitude0
? (C;C) (C;T) (T;T) 28
deafness
OMIM612780
DescSEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND
Variant
Relatedalso
GWAS snp
PMID [PMID 22492993OA-icon.png]
Trait
Title C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans.
Risk Allele
P-val 2E-13
Odds Ratio 0.4400 None