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rs121909638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909638(C;C)
Make rs121909638(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38421853
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909638
ebirs121909638
HLIrs121909638
Exacrs121909638
Varsomers121909638
Maprs121909638
PheGenIrs121909638
hapmaprs121909638
1000 genomesrs121909638
hgdprs121909638
ensemblrs121909638
gopubmedrs121909638
geneviewrs121909638
scholarrs121909638
googlers121909638
pharmgkbrs121909638
gwascentralrs121909638
openSNPrs121909638
23andMers121909638
23andMe allrs121909638
SNP Nexus

SNPshotrs121909638
SNPdbers121909638
MSV3drs121909638
GWAS Ctlgrs121909638
Max Magnitude0
OMIM136350
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121909638(C;C)
Alt rs121909638(C;C)
Reference rs121909638(T;T)
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.38279371A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000030933.2,