rs587776981

Orientation

plus

Stabilized

minus

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

Make rs587776981(C;T)

Make rs587776981(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

142315063

Gene

SPRY4

is a	snp
is	mentioned by
dbSNP	rs587776981
dbSNP (classic)	rs587776981
ClinGen	rs587776981
ebi	rs587776981
HLI	rs587776981
Exac	rs587776981
Gnomad	rs587776981
Varsome	rs587776981
LitVar	rs587776981
Map	rs587776981
PheGenI	rs587776981
Biobank	rs587776981
1000 genomes	rs587776981
hgdp	rs587776981
ensembl	rs587776981
geneview	rs587776981
scholar	rs587776981
google	rs587776981
pharmgkb	rs587776981
gwascentral	rs587776981
openSNP	rs587776981
23andMe	rs587776981
SNPshot	rs587776981
SNPdbe	rs587776981
MSV3d	rs587776981
GWAS Ctlg	rs587776981

Max Magnitude

0

ClinVar
Risk	Rs587776981(C;C) rs587776981(T;T)
Alt	Rs587776981(C;C) rs587776981(T;T)
Reference	Rs587776981(G;G)
Significance	Pathogenic
Disease	Hypogonadotropic hypogonadism 17 with or without anosmia
Variation	info
Gene	SPRY4
CLNDBN	Hypogonadotropic hypogonadism 17 with or without anosmia
Reversed	1
HGVS	NC_000005.9:g.141694628C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043617.3,