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rs587776885

From SNPedia

Orientationplus
Geno Mag Summary
(GCTGC;GCTGC) 0 common in clinvar
Make rs587776885(-;-)
Make rs587776885(-;GCGCT)
Make rs587776885(GCGCT;GCGCT)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position111418748
GeneSH2B3
is asnp
is mentioned by
dbSNPrs587776885
ebirs587776885
HLIrs587776885
Exacrs587776885
Varsomers587776885
Maprs587776885
PheGenIrs587776885
hapmaprs587776885
1000 genomesrs587776885
hgdprs587776885
ensemblrs587776885
gopubmedrs587776885
geneviewrs587776885
scholarrs587776885
googlers587776885
pharmgkbrs587776885
gwascentralrs587776885
openSNPrs587776885
23andMers587776885
23andMe allrs587776885
SNP Nexus

SNPshotrs587776885
SNPdbers587776885
MSV3drs587776885
GWAS Ctlgrs587776885
Max Magnitude0
ClinVar
Risk rs587776885(;)
Alt rs587776885(;)
Reference rs587776885(GCTGC;GCTGC)
Significance Pathogenic
Disease Myelofibrosis
Variation info
Gene SH2B3
CLNDBN Myelofibrosis
Reversed 0
HGVS NC_000012.11:g.111856552_111856556delGCGCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000023397.4,