rs34911341
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs34911341(C;T) |
Make rs34911341(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 10289835 |
Gene | GHRL, GHRLOS |
is a | snp |
is | mentioned by |
dbSNP | rs34911341 |
dbSNP (classic) | rs34911341 |
ClinGen | rs34911341 |
ebi | rs34911341 |
HLI | rs34911341 |
Exac | rs34911341 |
Gnomad | rs34911341 |
Varsome | rs34911341 |
LitVar | rs34911341 |
Map | rs34911341 |
PheGenI | rs34911341 |
Biobank | rs34911341 |
1000 genomes | rs34911341 |
hgdp | rs34911341 |
ensembl | rs34911341 |
geneview | rs34911341 |
scholar | rs34911341 |
rs34911341 | |
pharmgkb | rs34911341 |
gwascentral | rs34911341 |
openSNP | rs34911341 |
23andMe | rs34911341 |
SNPshot | rs34911341 |
SNPdbe | rs34911341 |
MSV3d | rs34911341 |
GWAS Ctlg | rs34911341 |
GMAF | 0.002755 |
Max Magnitude | 0 |
[PMID 20010782] Influence of ghrelin gene polymorphisms on hypertension and atherosclerotic disease
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 21448464] The ghrelin signalling system is involved in the consumption of sweets.