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rs121909642

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909642(C;T)
Make rs121909642(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38414174
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909642
ebirs121909642
HLIrs121909642
Exacrs121909642
Varsomers121909642
Maprs121909642
PheGenIrs121909642
hapmaprs121909642
1000 genomesrs121909642
hgdprs121909642
ensemblrs121909642
gopubmedrs121909642
geneviewrs121909642
scholarrs121909642
googlers121909642
pharmgkbrs121909642
gwascentralrs121909642
openSNPrs121909642
23andMers121909642
23andMe allrs121909642
SNP Nexus

SNPshotrs121909642
SNPdbers121909642
MSV3drs121909642
GWAS Ctlgrs121909642
Max Magnitude0
OMIM136350
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121909642(T;T)
Alt rs121909642(T;T)
Reference rs121909642(C;C)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 2 with anosmia
Variation info
Gene FGFR1
CLNDBN Hypogonadotropic hypogonadism 2 with anosmia
Reversed 1
HGVS NC_000008.10:g.38271692G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030937.27,