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rs879253721

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879253721(A;G)
Make rs879253721(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position121517316
GeneFGFR2
is asnp
is mentioned by
dbSNPrs879253721
ebirs879253721
HLIrs879253721
Exacrs879253721
Varsomers879253721
Maprs879253721
PheGenIrs879253721
hapmaprs879253721
1000 genomesrs879253721
hgdprs879253721
ensemblrs879253721
gopubmedrs879253721
geneviewrs879253721
scholarrs879253721
googlers879253721
pharmgkbrs879253721
gwascentralrs879253721
openSNPrs879253721
23andMers879253721
23andMe allrs879253721
SNP Nexus

SNPshotrs879253721
SNPdbers879253721
MSV3drs879253721
GWAS Ctlgrs879253721
Max Magnitude0
ClinVar
Risk rs879253721(G;G)
Alt rs879253721(G;G)
Reference rs879253721(A;A)
Significance Pathogenic
Disease Pfeiffer syndrome Crouzon syndrome
Variation info
Gene FGFR2
CLNDBN Pfeiffer syndrome Crouzon syndrome
Reversed 1
HGVS NC_000010.10:g.123276830T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014225.24, RCV000014226.25,