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rs199544087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199544087(A;A)
Make rs199544087(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position1805761
GeneFGFR3
is asnp
is mentioned by
dbSNPrs199544087
dbSNP (old)rs199544087
ClinGenrs199544087
ebirs199544087
HLIrs199544087
Exacrs199544087
Gnomadrs199544087
Varsomers199544087
Maprs199544087
PheGenIrs199544087
Biobankrs199544087
1000 genomesrs199544087
hgdprs199544087
ensemblrs199544087
gopubmedrs199544087
geneviewrs199544087
scholarrs199544087
googlers199544087
pharmgkbrs199544087
gwascentralrs199544087
openSNPrs199544087
23andMers199544087
23andMe allrs199544087
SNPshotrs199544087
SNPdbers199544087
MSV3drs199544087
GWAS Ctlgrs199544087
Max Magnitude0
ClinVar
Risk rs199544087(A;A) rs199544087(T;T)
Alt rs199544087(A;A) rs199544087(T;T)
Reference Rs199544087(G;G)
Significance Probable-Pathogenic
Disease Myeloproliferative disorder
Variation info
Gene FGFR3
CLNDBN Myeloproliferative disorder
Reversed 0
HGVS NC_000004.11:g.1807488G>A
CLNSRC
CLNACC RCV000418578.1,