Rs121918487

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918487(A;A)
Make rs121918487(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position121517378
GeneFGFR2
is asnp
is mentioned by
dbSNPrs121918487
PheGenIrs121918487
nextbiors121918487
hapmaprs121918487
1000 genomesrs121918487
hgdprs121918487
ensemblrs121918487
gopubmedrs121918487
geneviewrs121918487
scholarrs121918487
googlers121918487
pharmgkbrs121918487
gwascentralrs121918487
openSNPrs121918487
23andMers121918487
23andMe allrs121918487
SNP Nexus

SNPshotrs121918487
SNPdbers121918487
MSV3drs121918487
Max Magnitude0
OMIM176943
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918487(A;A)
Alt rs121918487(A;A)
Reference rs121918487(G;G)
Significance Pathogenic
Disease Crouzon syndrome Pfeiffer syndrome
Variation info
Gene FGFR2
CLNDBN Crouzon syndrome Pfeiffer syndrome
Reversed 1
HGVS NC_000010.10:g.123276892C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014173.16, RCV000014174.24,