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rs387906678

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906678(G;G)
Make rs387906678(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position121515263
GeneFGFR2
is asnp
is mentioned by
dbSNPrs387906678
ebirs387906678
HLIrs387906678
Exacrs387906678
Varsomers387906678
Maprs387906678
PheGenIrs387906678
hapmaprs387906678
1000 genomesrs387906678
hgdprs387906678
ensemblrs387906678
gopubmedrs387906678
geneviewrs387906678
scholarrs387906678
googlers387906678
pharmgkbrs387906678
gwascentralrs387906678
openSNPrs387906678
23andMers387906678
23andMe allrs387906678
SNP Nexus

SNPshotrs387906678
SNPdbers387906678
MSV3drs387906678
GWAS Ctlgrs387906678
Max Magnitude0
ClinVar
Risk rs387906678(G;G)
Alt rs387906678(G;G)
Reference rs387906678(T;T)
Significance Pathogenic
Disease Bent bone dysplasia syndrome Inborn genetic diseases
Variation info
Gene FGFR2
CLNDBN Bent bone dysplasia syndrome Inborn genetic diseases
Reversed 1
HGVS NC_000010.10:g.123274777A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022735.23, RCV000190765.1,