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rs587776980

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776980(G;T)
Make rs587776980(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position57097973
GeneIL17RD
is asnp
is mentioned by
dbSNPrs587776980
ebirs587776980
HLIrs587776980
Exacrs587776980
Varsomers587776980
Maprs587776980
PheGenIrs587776980
hapmaprs587776980
1000 genomesrs587776980
hgdprs587776980
ensemblrs587776980
gopubmedrs587776980
geneviewrs587776980
scholarrs587776980
googlers587776980
pharmgkbrs587776980
gwascentralrs587776980
openSNPrs587776980
23andMers587776980
23andMe allrs587776980
SNP Nexus

SNPshotrs587776980
SNPdbers587776980
MSV3drs587776980
GWAS Ctlgrs587776980
Max Magnitude0
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
CLNACC RCV000043613.2,