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rs1824938

From SNPedia

Orientationminus
Stabilizedminus
Make rs1824938(C;C)
Make rs1824938(C;T)
Make rs1824938(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position5091915
is asnp
is mentioned by
dbSNPrs1824938
ebirs1824938
HLIrs1824938
Exacrs1824938
Varsomers1824938
Maprs1824938
PheGenIrs1824938
hapmaprs1824938
1000 genomesrs1824938
hgdprs1824938
ensemblrs1824938
gopubmedrs1824938
geneviewrs1824938
scholarrs1824938
googlers1824938
pharmgkbrs1824938
gwascentralrs1824938
openSNPrs1824938
23andMers1824938
23andMe allrs1824938
SNP Nexus

SNPshotrs1824938
SNPdbers1824938
MSV3drs1824938
GWAS Ctlgrs1824938
GMAF0.2516
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM611091
DescMENTAL RETARDATION, AUTOSOMAL RECESSIVE 5; MRT5
Variant
Relatedalso
[PMID 17903302OA-icon.png] Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.