rs587776980

Orientation

plus

Stabilized

plus

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

Make rs587776980(G;T)

Make rs587776980(T;T)

Reference

GRCh38 38.1/142

Chromosome

3

Position

57097973

Gene

IL17RD

is a	snp
is	mentioned by
dbSNP	rs587776980
dbSNP (classic)	rs587776980
ClinGen	rs587776980
ebi	rs587776980
HLI	rs587776980
Exac	rs587776980
Gnomad	rs587776980
Varsome	rs587776980
LitVar	rs587776980
Map	rs587776980
PheGenI	rs587776980
Biobank	rs587776980
1000 genomes	rs587776980
hgdp	rs587776980
ensembl	rs587776980
geneview	rs587776980
scholar	rs587776980
google	rs587776980
pharmgkb	rs587776980
gwascentral	rs587776980
openSNP	rs587776980
23andMe	rs587776980
SNPshot	rs587776980
SNPdbe	rs587776980
MSV3d	rs587776980
GWAS Ctlg	rs587776980

Max Magnitude

0

ClinVar
Risk	rs587776980(T;T)
Alt	rs587776980(T;T)
Reference	Rs587776980(G;G)
Significance	Pathogenic
Disease	Hypogonadotropic hypogonadism 18 with anosmia
Variation	info
Gene	IL17RD
CLNDBN	Hypogonadotropic hypogonadism 18 with anosmia
Reversed	0
HGVS	NC_000003.11:g.57132001G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000043613.2,