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rs587778773

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778773(C;T)
Make rs587778773(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position1801886
GeneFGFR3
is asnp
is mentioned by
dbSNPrs587778773
ebirs587778773
HLIrs587778773
Exacrs587778773
Varsomers587778773
Maprs587778773
PheGenIrs587778773
hapmaprs587778773
1000 genomesrs587778773
hgdprs587778773
ensemblrs587778773
gopubmedrs587778773
geneviewrs587778773
scholarrs587778773
googlers587778773
pharmgkbrs587778773
gwascentralrs587778773
openSNPrs587778773
23andMers587778773
23andMe allrs587778773
SNP Nexus

SNPshotrs587778773
SNPdbers587778773
MSV3drs587778773
GWAS Ctlgrs587778773
Max Magnitude0
ClinVar
Risk rs587778773(T;T)
Alt rs587778773(T;T)
Reference rs587778773(C;C)
Significance Pathogenic
Disease Hypochondroplasia
Variation info
Gene FGFR3
CLNDBN Hypochondroplasia
Reversed 0
HGVS NC_000004.11:g.1803613C>T
CLNSRC
CLNACC RCV000056063.1,