rs104893841

Orientation

minus

Stabilized

minus

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

Make rs104893841(A;A)

Make rs104893841(A;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

67740526

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs104893841
dbSNP (classic)	rs104893841
ClinGen	rs104893841
ebi	rs104893841
HLI	rs104893841
Exac	rs104893841
Gnomad	rs104893841
Varsome	rs104893841
LitVar	rs104893841
Map	rs104893841
PheGenI	rs104893841
Biobank	rs104893841
1000 genomes	rs104893841
hgdp	rs104893841
ensembl	rs104893841
geneview	rs104893841
scholar	rs104893841
google	rs104893841
pharmgkb	rs104893841
gwascentral	rs104893841
openSNP	rs104893841
23andMe	rs104893841
SNPshot	rs104893841
SNPdbe	rs104893841
MSV3d	rs104893841
GWAS Ctlg	rs104893841

Max Magnitude

0

OMIM	138850
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104893841(A;A)
Alt	rs104893841(A;A)
Reference	Rs104893841(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.68606244A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030913.29,