rs776834867

Orientation

plus

Stabilized

plus

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

Make rs776834867(G;T)

Make rs776834867(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

67754305

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs776834867
dbSNP (classic)	rs776834867
ClinGen	rs776834867
ebi	rs776834867
HLI	rs776834867
Exac	rs776834867
Gnomad	rs776834867
Varsome	rs776834867
LitVar	rs776834867
Map	rs776834867
PheGenI	rs776834867
Biobank	rs776834867
1000 genomes	rs776834867
hgdp	rs776834867
ensembl	rs776834867
geneview	rs776834867
scholar	rs776834867
google	rs776834867
pharmgkb	rs776834867
gwascentral	rs776834867
openSNP	rs776834867
23andMe	rs776834867
SNPshot	rs776834867
SNPdbe	rs776834867
MSV3d	rs776834867
GWAS Ctlg	rs776834867

Max Magnitude

0

ClinVar
Risk	rs776834867(T;T)
Alt	rs776834867(T;T)
Reference	Rs776834867(G;G)
Significance	Probable-Pathogenic
Disease	Isolated GnRH Deficiency
Variation	info
Gene	GNRHR
CLNDBN	Isolated GnRH Deficiency
Reversed	0
HGVS	NC_000004.11:g.68620023G>T
CLNSRC	Illumina
CLNACC	RCV000318227.1,