rs202080221

Orientation

plus

Stabilized

plus

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

Make rs202080221(C;C)

Make rs202080221(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

111418767

Gene

SH2B3

is a	snp
is	mentioned by
dbSNP	rs202080221
dbSNP (classic)	rs202080221
ClinGen	rs202080221
ebi	rs202080221
HLI	rs202080221
Exac	rs202080221
Gnomad	rs202080221
Varsome	rs202080221
LitVar	rs202080221
Map	rs202080221
PheGenI	rs202080221
Biobank	rs202080221
1000 genomes	rs202080221
hgdp	rs202080221
ensembl	rs202080221
geneview	rs202080221
scholar	rs202080221
google	rs202080221
pharmgkb	rs202080221
gwascentral	rs202080221
openSNP	rs202080221
23andMe	rs202080221
SNPshot	rs202080221
SNPdbe	rs202080221
MSV3d	rs202080221
GWAS Ctlg	rs202080221

Max Magnitude

0

ClinVar
Risk	rs202080221(C;C) rs202080221(T;T)
Alt	rs202080221(C;C) rs202080221(T;T)
Reference	Rs202080221(G;G)
Significance	Other
Disease	Essential thrombocythemia Familial erythrocytosis
Variation	info
Gene	SH2B3
CLNDBN	Essential thrombocythemia Familial erythrocytosis, 1
Reversed	0
HGVS	NC_000012.11:g.111856571G>C; NC_000012.11:g.111856571G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023398.4, RCV000023399.5,