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rs149182247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149182247(C;T)
Make rs149182247(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position30976461
GeneGHRHR
is asnp
is mentioned by
dbSNPrs149182247
dbSNP (classic)rs149182247
ClinGenrs149182247
ebirs149182247
HLIrs149182247
Exacrs149182247
Gnomadrs149182247
Varsomers149182247
LitVarrs149182247
Maprs149182247
PheGenIrs149182247
Biobankrs149182247
1000 genomesrs149182247
hgdprs149182247
ensemblrs149182247
geneviewrs149182247
scholarrs149182247
googlers149182247
pharmgkbrs149182247
gwascentralrs149182247
openSNPrs149182247
23andMers149182247
23andMe allrs149182247
SNPshotrs149182247
SNPdbers149182247
MSV3drs149182247
GWAS Ctlgrs149182247
Max Magnitude0
ClinVar
Risk rs149182247(T;T)
Alt rs149182247(T;T)
Reference Rs149182247(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GHRHR
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.31016076C>T
CLNSRC
CLNACC RCV000489482.1,