rs149182247

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs149182247(C;T)

Make rs149182247(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

30976461

Gene

GHRHR

is a	snp
is	mentioned by
dbSNP	rs149182247
dbSNP (classic)	rs149182247
ClinGen	rs149182247
ebi	rs149182247
HLI	rs149182247
Exac	rs149182247
Gnomad	rs149182247
Varsome	rs149182247
LitVar	rs149182247
Map	rs149182247
PheGenI	rs149182247
Biobank	rs149182247
1000 genomes	rs149182247
hgdp	rs149182247
ensembl	rs149182247
geneview	rs149182247
scholar	rs149182247
google	rs149182247
pharmgkb	rs149182247
gwascentral	rs149182247
openSNP	rs149182247
23andMe	rs149182247
SNPshot	rs149182247
SNPdbe	rs149182247
MSV3d	rs149182247
GWAS Ctlg	rs149182247

Max Magnitude

0

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,