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rs121909639

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909639(C;T)
Make rs121909639(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38415899
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909639
ebirs121909639
HLIrs121909639
Exacrs121909639
Varsomers121909639
Maprs121909639
PheGenIrs121909639
hapmaprs121909639
1000 genomesrs121909639
hgdprs121909639
ensemblrs121909639
gopubmedrs121909639
geneviewrs121909639
scholarrs121909639
googlers121909639
pharmgkbrs121909639
gwascentralrs121909639
openSNPrs121909639
23andMers121909639
23andMe allrs121909639
SNP Nexus

SNPshotrs121909639
SNPdbers121909639
MSV3drs121909639
GWAS Ctlgrs121909639
Max Magnitude0
OMIM136350
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121909639(T;T)
Alt rs121909639(T;T)
Reference rs121909639(C;C)
Significance Other
Disease HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
Variation info
Gene FGFR1
CLNDBN HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO
Reversed 1
HGVS NC_000008.10:g.38273417G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030934.2,