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rs34911341

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34911341(C;T)
Make rs34911341(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10289835
GeneGHRL, GHRLOS
is asnp
is mentioned by
dbSNPrs34911341
ebirs34911341
HLIrs34911341
Exacrs34911341
Varsomers34911341
Maprs34911341
PheGenIrs34911341
hapmaprs34911341
1000 genomesrs34911341
hgdprs34911341
ensemblrs34911341
gopubmedrs34911341
geneviewrs34911341
scholarrs34911341
googlers34911341
pharmgkbrs34911341
gwascentralrs34911341
openSNPrs34911341
23andMers34911341
23andMe allrs34911341
SNP Nexus

SNPshotrs34911341
SNPdbers34911341
MSV3drs34911341
GWAS Ctlgrs34911341
GMAF0.002755
Max Magnitude0

[PMID 20010782] Influence of ghrelin gene polymorphisms on hypertension and atherosclerotic disease

OMIM605353
Desc
Variant0001
Relatedalso


ClinVar
Risk rs34911341(T;T)
Alt rs34911341(T;T)
Reference rs34911341(C;C)
Significance Other
Disease Metabolic syndrome Obesity
Variation info
Gene GHRLOS GHRL
CLNDBN Metabolic syndrome, susceptibility to Obesity
Reversed 0
HGVS NC_000003.11:g.10331519C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005364.2, RCV000033194.2,



[PMID 20152820] The ghrelin gene allele 51Q (rs34911341) is a protective factor against the development of gestational diabetes.


[PMID 21448464OA-icon.png] The ghrelin signalling system is involved in the consumption of sweets.