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rs121909637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909637(G;T)
Make rs121909637(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38418249
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909637
ebirs121909637
HLIrs121909637
Exacrs121909637
Varsomers121909637
Maprs121909637
PheGenIrs121909637
hapmaprs121909637
1000 genomesrs121909637
hgdprs121909637
ensemblrs121909637
gopubmedrs121909637
geneviewrs121909637
scholarrs121909637
googlers121909637
pharmgkbrs121909637
gwascentralrs121909637
openSNPrs121909637
23andMers121909637
23andMe allrs121909637
SNP Nexus

SNPshotrs121909637
SNPdbers121909637
MSV3drs121909637
GWAS Ctlgrs121909637
Max Magnitude0
OMIM136350
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121909637(A,T;A,T)
Alt rs121909637(A,T;A,T)
Reference rs121909637(G;G)
Significance Other
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 1
HGVS NC_000008.10:g.38275767C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030932.3,