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rs587777857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777857(A;A)
Make rs587777857(A;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position1805661
GeneFGFR3
is asnp
is mentioned by
dbSNPrs587777857
ebirs587777857
HLIrs587777857
Exacrs587777857
Varsomers587777857
Maprs587777857
PheGenIrs587777857
hapmaprs587777857
1000 genomesrs587777857
hgdprs587777857
ensemblrs587777857
gopubmedrs587777857
geneviewrs587777857
scholarrs587777857
googlers587777857
pharmgkbrs587777857
gwascentralrs587777857
openSNPrs587777857
23andMers587777857
23andMe allrs587777857
SNP Nexus

SNPshotrs587777857
SNPdbers587777857
MSV3drs587777857
GWAS Ctlgrs587777857
Max Magnitude0
ClinVar
Risk rs587777857(A;A)
Alt rs587777857(A;A)
Reference rs587777857(C;C)
Significance Pathogenic
Disease Camptodactyly
Variation info
Gene FGFR3
CLNDBN Camptodactyly, tall stature, and hearing loss syndrome
Reversed 0
HGVS NC_000004.11:g.1807388C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144699.3,