rs587776885

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GCTGC;GCTGC)	0	common in clinvar

Make rs587776885(-;-)

Make rs587776885(-;GCGCT)

Make rs587776885(GCGCT;GCGCT)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

111418748

Gene

SH2B3

is a	snp
is	mentioned by
dbSNP	rs587776885
dbSNP (classic)	rs587776885
ClinGen	rs587776885
ebi	rs587776885
HLI	rs587776885
Exac	rs587776885
Gnomad	rs587776885
Varsome	rs587776885
LitVar	rs587776885
Map	rs587776885
PheGenI	rs587776885
Biobank	rs587776885
1000 genomes	rs587776885
hgdp	rs587776885
ensembl	rs587776885
geneview	rs587776885
scholar	rs587776885
google	rs587776885
pharmgkb	rs587776885
gwascentral	rs587776885
openSNP	rs587776885
23andMe	rs587776885
SNPshot	rs587776885
SNPdbe	rs587776885
MSV3d	rs587776885
GWAS Ctlg	rs587776885

Max Magnitude

0

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,