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rs398123026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123026(A;G)
Make rs398123026(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position22048158
GeneFGF17
is asnp
is mentioned by
dbSNPrs398123026
ebirs398123026
HLIrs398123026
Exacrs398123026
Varsomers398123026
Maprs398123026
PheGenIrs398123026
hapmaprs398123026
1000 genomesrs398123026
hgdprs398123026
ensemblrs398123026
gopubmedrs398123026
geneviewrs398123026
scholarrs398123026
googlers398123026
pharmgkbrs398123026
gwascentralrs398123026
openSNPrs398123026
23andMers398123026
23andMe allrs398123026
SNP Nexus

SNPshotrs398123026
SNPdbers398123026
MSV3drs398123026
GWAS Ctlgrs398123026
Max Magnitude0
ClinVar
Risk rs398123026(G;G)
Alt rs398123026(G;G)
Reference rs398123026(A;A)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 20 with or without anosmia
Variation info
Gene DMTN FGF17
CLNDBN Hypogonadotropic hypogonadism 20 with or without anosmia
Reversed 0
HGVS NC_000008.10:g.21905669A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000043600.3,