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rs121909632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909632(A;T)
Make rs121909632(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38421889
GeneFGFR1
is asnp
is mentioned by
dbSNPrs121909632
ebirs121909632
HLIrs121909632
Exacrs121909632
Varsomers121909632
Maprs121909632
PheGenIrs121909632
hapmaprs121909632
1000 genomesrs121909632
hgdprs121909632
ensemblrs121909632
gopubmedrs121909632
geneviewrs121909632
scholarrs121909632
googlers121909632
pharmgkbrs121909632
gwascentralrs121909632
openSNPrs121909632
23andMers121909632
23andMe allrs121909632
SNP Nexus

SNPshotrs121909632
SNPdbers121909632
MSV3drs121909632
GWAS Ctlgrs121909632
Max Magnitude0
OMIM136350
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909632(T;T)
Alt rs121909632(T;T)
Reference rs121909632(A;A)
Significance Pathogenic
Disease Osteoglophonic dysplasia
Variation info
Gene FGFR1
CLNDBN Osteoglophonic dysplasia
Reversed 1
HGVS NC_000008.10:g.38279407T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017678.28,