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rs368927897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368927897(G;T)
Make rs368927897(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position5072541
GeneINSL6, JAK2
is asnp
is mentioned by
dbSNPrs368927897
dbSNP (classic)rs368927897
ClinGenrs368927897
ebirs368927897
HLIrs368927897
Exacrs368927897
Gnomadrs368927897
Varsomers368927897
LitVarrs368927897
Maprs368927897
PheGenIrs368927897
Biobankrs368927897
1000 genomesrs368927897
hgdprs368927897
ensemblrs368927897
geneviewrs368927897
scholarrs368927897
googlers368927897
pharmgkbrs368927897
gwascentralrs368927897
openSNPrs368927897
23andMers368927897
SNPshotrs368927897
SNPdbers368927897
MSV3drs368927897
GWAS Ctlgrs368927897
Max Magnitude0
ClinVar
Risk rs368927897(T;T)
Alt rs368927897(T;T)
Reference Rs368927897(G;G)
Significance Probable-Pathogenic
Disease Myeloproliferative disorder
Variation info
Gene JAK2
CLNDBN Myeloproliferative disorder
Reversed 0
HGVS NC_000009.11:g.5072541G>T
CLNSRC
CLNACC RCV000418120.1,