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rs121909628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909628(C;T)
Make rs121909628(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38414892
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909628
ebirs121909628
HLIrs121909628
Exacrs121909628
Varsomers121909628
Maprs121909628
PheGenIrs121909628
hapmaprs121909628
1000 genomesrs121909628
hgdprs121909628
ensemblrs121909628
gopubmedrs121909628
geneviewrs121909628
scholarrs121909628
googlers121909628
pharmgkbrs121909628
gwascentralrs121909628
openSNPrs121909628
23andMers121909628
23andMe allrs121909628
SNP Nexus

SNPshotrs121909628
SNPdbers121909628
MSV3drs121909628
GWAS Ctlgrs121909628
Max Magnitude0
OMIM136350
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909628(T;T)
Alt rs121909628(T;T)
Reference rs121909628(C;C)
Significance Other
Disease Kallmann syndrome 2 Hypogonadotrophic hypogonadism Delayed puberty
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2 Hypogonadotrophic hypogonadism Delayed puberty
Reversed 1
HGVS NC_000008.10:g.38272410G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030926.4, RCV000156953.1, RCV000156954.1,