rs104893844

Orientation

minus

Stabilized

minus

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

Make rs104893844(A;A)

Make rs104893844(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

67754068

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs104893844
dbSNP (classic)	rs104893844
ClinGen	rs104893844
ebi	rs104893844
HLI	rs104893844
Exac	rs104893844
Gnomad	rs104893844
Varsome	rs104893844
LitVar	rs104893844
Map	rs104893844
PheGenI	rs104893844
Biobank	rs104893844
1000 genomes	rs104893844
hgdp	rs104893844
ensembl	rs104893844
geneview	rs104893844
scholar	rs104893844
google	rs104893844
pharmgkb	rs104893844
gwascentral	rs104893844
openSNP	rs104893844
23andMe	rs104893844
SNPshot	rs104893844
SNPdbe	rs104893844
MSV3d	rs104893844
GWAS Ctlg	rs104893844

Max Magnitude

0

OMIM	138850
Desc
Variant	0010
Related	also

ClinVar
Risk	rs104893844(A;A)
Alt	rs104893844(A;A)
Reference	Rs104893844(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	1
HGVS	NC_000004.11:g.68619786C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030916.24,