rs606231406

Orientation

minus

Stabilized

minus

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

Make rs606231406(C;C)

Make rs606231406(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

67753944

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs606231406
dbSNP (classic)	rs606231406
ClinGen	rs606231406
ebi	rs606231406
HLI	rs606231406
Exac	rs606231406
Gnomad	rs606231406
Varsome	rs606231406
LitVar	rs606231406
Map	rs606231406
PheGenI	rs606231406
Biobank	rs606231406
1000 genomes	rs606231406
hgdp	rs606231406
ensembl	rs606231406
geneview	rs606231406
scholar	rs606231406
google	rs606231406
pharmgkb	rs606231406
gwascentral	rs606231406
openSNP	rs606231406
23andMe	rs606231406
SNPshot	rs606231406
SNPdbe	rs606231406
MSV3d	rs606231406
GWAS Ctlg	rs606231406

Max Magnitude

0

ClinVar
Risk	rs606231406(C;C)
Alt	rs606231406(C;C)
Reference	Rs606231406(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	1
HGVS	NC_000004.11:g.68619662A>G
CLNSRC
CLNACC	RCV000128826.1,