rs104893839

Orientation

minus

Stabilized

minus

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

Make rs104893839(A;A)

Make rs104893839(A;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

67744659

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs104893839
dbSNP (classic)	rs104893839
ClinGen	rs104893839
ebi	rs104893839
HLI	rs104893839
Exac	rs104893839
Gnomad	rs104893839
Varsome	rs104893839
LitVar	rs104893839
Map	rs104893839
PheGenI	rs104893839
Biobank	rs104893839
1000 genomes	rs104893839
hgdp	rs104893839
ensembl	rs104893839
geneview	rs104893839
scholar	rs104893839
google	rs104893839
pharmgkb	rs104893839
gwascentral	rs104893839
openSNP	rs104893839
23andMe	rs104893839
SNPshot	rs104893839
SNPdbe	rs104893839
MSV3d	rs104893839
GWAS Ctlg	rs104893839

Max Magnitude

0

OMIM	138850
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104893839(A;A)
Alt	rs104893839(A;A)
Reference	Rs104893839(C;C)
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.68610377G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030911.29,