rs104893843

Orientation

minus

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

Make rs104893843(A;A)

Make rs104893843(A;T)

Reference

GRCh37 37.1/132

Chromosome

4

Position

68620024

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs104893843
dbSNP (classic)	rs104893843
ClinGen	rs104893843
ebi	rs104893843
HLI	rs104893843
Exac	rs104893843
Gnomad	rs104893843
Varsome	rs104893843
LitVar	rs104893843
Map	rs104893843
PheGenI	rs104893843
Biobank	rs104893843
1000 genomes	rs104893843
hgdp	rs104893843
ensembl	rs104893843
geneview	rs104893843
scholar	rs104893843
google	rs104893843
pharmgkb	rs104893843
gwascentral	rs104893843
openSNP	rs104893843
23andMe	rs104893843
SNPshot	rs104893843
SNPdbe	rs104893843
MSV3d	rs104893843
GWAS Ctlg	rs104893843

Max Magnitude

0

OMIM	138850
Desc
Variant	0009
Related	also

ClinVar
Risk	rs104893843(A;A)
Alt	rs104893843(A;A)
Reference	Rs104893843(T;T)
Significance	Pathogenic
Disease	Hypogonadotropic hypogonadism
Variation	info
Gene	GNRHR
CLNDBN	Hypogonadotropic hypogonadism
Reversed	1
HGVS	NC_000004.11:g.68620024A>T
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000037678.1,