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rs121909641

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909641(C;T)
Make rs121909641(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38419720
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909641
ebirs121909641
HLIrs121909641
Exacrs121909641
Varsomers121909641
Maprs121909641
PheGenIrs121909641
hapmaprs121909641
1000 genomesrs121909641
hgdprs121909641
ensemblrs121909641
gopubmedrs121909641
geneviewrs121909641
scholarrs121909641
googlers121909641
pharmgkbrs121909641
gwascentralrs121909641
openSNPrs121909641
23andMers121909641
23andMe allrs121909641
SNP Nexus

SNPshotrs121909641
SNPdbers121909641
MSV3drs121909641
GWAS Ctlgrs121909641
Max Magnitude0
OMIM136350
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121909641(T;T)
Alt rs121909641(T;T)
Reference rs121909641(C;C)
Significance Other
Disease HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA Hypogonadotrophic hypogonadism
Variation info
Gene FGFR1
CLNDBN HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO Hypogonadotrophic hypogonadism
Reversed 1
HGVS NC_000008.10:g.38277238G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030936.3, RCV000156970.1,