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rs121909640

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909640(A;A)
Make rs121909640(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position38429898
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909640
ebirs121909640
HLIrs121909640
Exacrs121909640
Varsomers121909640
Maprs121909640
PheGenIrs121909640
hapmaprs121909640
1000 genomesrs121909640
hgdprs121909640
ensemblrs121909640
gopubmedrs121909640
geneviewrs121909640
scholarrs121909640
googlers121909640
pharmgkbrs121909640
gwascentralrs121909640
openSNPrs121909640
23andMers121909640
23andMe allrs121909640
SNP Nexus

SNPshotrs121909640
SNPdbers121909640
MSV3drs121909640
GWAS Ctlgrs121909640
Max Magnitude0
OMIM136350
Desc
Variant0020
Relatedalso
ClinVar
Risk rs121909640(A;A)
Alt rs121909640(A;A)
Reference rs121909640(G;G)
Significance Pathogenic
Disease Kallmann syndrome 2
Variation info
Gene FGFR1
CLNDBN Kallmann syndrome 2
Reversed 1
HGVS NC_000008.10:g.38287416C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017691.27,