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rs121909634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909634(C;C)
Make rs121909634(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38419676
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909634
ebirs121909634
HLIrs121909634
Exacrs121909634
Varsomers121909634
Maprs121909634
PheGenIrs121909634
hapmaprs121909634
1000 genomesrs121909634
hgdprs121909634
ensemblrs121909634
gopubmedrs121909634
geneviewrs121909634
scholarrs121909634
googlers121909634
pharmgkbrs121909634
gwascentralrs121909634
openSNPrs121909634
23andMers121909634
23andMe allrs121909634
SNP Nexus

SNPshotrs121909634
SNPdbers121909634
MSV3drs121909634
GWAS Ctlgrs121909634
Max Magnitude0
OMIM136350
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121909634(C;C)
Alt rs121909634(C;C)
Reference rs121909634(T;T)
Significance Pathogenic
Disease Osteoglophonic dysplasia
Variation info
Gene FGFR1
CLNDBN Osteoglophonic dysplasia
Reversed 1
HGVS NC_000008.10:g.38277194A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017682.25,