rs369176613

Orientation

plus

Stabilized

plus

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

Make rs369176613(A;A)

Make rs369176613(A;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

67740661

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs369176613
dbSNP (classic)	rs369176613
ClinGen	rs369176613
ebi	rs369176613
HLI	rs369176613
Exac	rs369176613
Gnomad	rs369176613
Varsome	rs369176613
LitVar	rs369176613
Map	rs369176613
PheGenI	rs369176613
Biobank	rs369176613
1000 genomes	rs369176613
hgdp	rs369176613
ensembl	rs369176613
geneview	rs369176613
scholar	rs369176613
google	rs369176613
pharmgkb	rs369176613
gwascentral	rs369176613
openSNP	rs369176613
23andMe	rs369176613
SNPshot	rs369176613
SNPdbe	rs369176613
MSV3d	rs369176613
GWAS Ctlg	rs369176613

Max Magnitude

0

ClinVar
Risk	rs369176613(A;A)
Alt	rs369176613(A;A)
Reference	Rs369176613(G;G)
Significance	Pathogenic
Disease	Hypogonadotropic hypogonadism 7 with or without anosmia
Variation	info
Gene	GNRHR
CLNDBN	Hypogonadotropic hypogonadism 7 with or without anosmia
Reversed	0
HGVS	NC_000004.11:g.68606379G>A
CLNSRC	ClinVar Seth G.S. Medical College and K.E.M. Hospital
CLNACC	RCV000128827.1, RCV000203470.1,