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rs1057517964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517964(C;G)
Make rs1057517964(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position1803813
GeneFGFR3
is asnp
is mentioned by
dbSNPrs1057517964
dbSNP (old)rs1057517964
ClinGenrs1057517964
ebirs1057517964
HLIrs1057517964
Exacrs1057517964
Gnomadrs1057517964
Varsomers1057517964
Maprs1057517964
PheGenIrs1057517964
Biobankrs1057517964
1000 genomesrs1057517964
hgdprs1057517964
ensemblrs1057517964
gopubmedrs1057517964
geneviewrs1057517964
scholarrs1057517964
googlers1057517964
pharmgkbrs1057517964
gwascentralrs1057517964
openSNPrs1057517964
23andMers1057517964
23andMe allrs1057517964
SNPshotrs1057517964
SNPdbers1057517964
MSV3drs1057517964
GWAS Ctlgrs1057517964
Max Magnitude0
ClinVar
Risk rs1057517964(G;G)
Alt rs1057517964(G;G)
Reference Rs1057517964(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR3
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.1805540C>G
CLNSRC
CLNACC RCV000413031.1,