rs515726219

Orientation

plus

Stabilized

plus

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

Make rs515726219(C;C)

Make rs515726219(C;T)

Reference

GRCh38 38.1/142

Chromosome

4

Position

67754242

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs515726219
dbSNP (classic)	rs515726219
ClinGen	rs515726219
ebi	rs515726219
HLI	rs515726219
Exac	rs515726219
Gnomad	rs515726219
Varsome	rs515726219
LitVar	rs515726219
Map	rs515726219
PheGenI	rs515726219
Biobank	rs515726219
1000 genomes	rs515726219
hgdp	rs515726219
ensembl	rs515726219
geneview	rs515726219
scholar	rs515726219
google	rs515726219
pharmgkb	rs515726219
gwascentral	rs515726219
openSNP	rs515726219
23andMe	rs515726219
SNPshot	rs515726219
SNPdbe	rs515726219
MSV3d	rs515726219
GWAS Ctlg	rs515726219

Max Magnitude

0

ClinVar
Risk	rs515726219(C;C)
Alt	rs515726219(C;C)
Reference	Rs515726219(T;T)
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.68619960T>C
CLNSRC	ClinVar Seth G.S. Medical College and K.E.M. Hospital
CLNACC	RCV000114425.1,