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rs398123025

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123025(A;A)
Make rs398123025(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position22048128
GeneFGF17
is asnp
is mentioned by
dbSNPrs398123025
ebirs398123025
HLIrs398123025
Exacrs398123025
Varsomers398123025
Maprs398123025
PheGenIrs398123025
hapmaprs398123025
1000 genomesrs398123025
hgdprs398123025
ensemblrs398123025
gopubmedrs398123025
geneviewrs398123025
scholarrs398123025
googlers398123025
pharmgkbrs398123025
gwascentralrs398123025
openSNPrs398123025
23andMers398123025
23andMe allrs398123025
SNP Nexus

SNPshotrs398123025
SNPdbers398123025
MSV3drs398123025
GWAS Ctlgrs398123025
Max Magnitude0
ClinVar
Risk rs398123025(A;A)
Alt rs398123025(A;A)
Reference rs398123025(G;G)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 20 without anosmia
Variation info
Gene DMTN FGF17
CLNDBN Hypogonadotropic hypogonadism 20 without anosmia
Reversed 0
HGVS NC_000008.10:g.21905639G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043599.3,