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rs779187338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779187338(C;T)
Make rs779187338(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position30971210
GeneGHRHR
is asnp
is mentioned by
dbSNPrs779187338
ClinGenrs779187338
ebirs779187338
HLIrs779187338
Exacrs779187338
Varsomers779187338
Maprs779187338
PheGenIrs779187338
hapmaprs779187338
1000 genomesrs779187338
hgdprs779187338
ensemblrs779187338
gopubmedrs779187338
geneviewrs779187338
scholarrs779187338
googlers779187338
pharmgkbrs779187338
gwascentralrs779187338
openSNPrs779187338
23andMers779187338
23andMe allrs779187338
SNP Nexus

SNPshotrs779187338
SNPdbers779187338
MSV3drs779187338
GWAS Ctlgrs779187338
Max Magnitude0
ClinVar
Risk rs779187338(A;A) rs779187338(T;T)
Alt rs779187338(A;A) rs779187338(T;T)
Reference Rs779187338(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GHRHR
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.31010825C>A
CLNSRC
CLNACC RCV000171528.1,