rs1057519960

Orientation

plus

Stabilized

plus

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

Make rs1057519960(A;G)

Make rs1057519960(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

66063413

Gene

SF3B2

is a	snp
is	mentioned by
dbSNP	rs1057519960
dbSNP (classic)	rs1057519960
ClinGen	rs1057519960
ebi	rs1057519960
HLI	rs1057519960
Exac	rs1057519960
Gnomad	rs1057519960
Varsome	rs1057519960
LitVar	rs1057519960
Map	rs1057519960
PheGenI	rs1057519960
Biobank	rs1057519960
1000 genomes	rs1057519960
hgdp	rs1057519960
ensembl	rs1057519960
geneview	rs1057519960
scholar	rs1057519960
google	rs1057519960
pharmgkb	rs1057519960
gwascentral	rs1057519960
openSNP	rs1057519960
23andMe	rs1057519960
SNPshot	rs1057519960
SNPdbe	rs1057519960
MSV3d	rs1057519960
GWAS Ctlg	rs1057519960

Max Magnitude

0

ClinVar
Risk	rs1057519960(G;G)
Alt	rs1057519960(G;G)
Reference	Rs1057519960(A;A)
Significance	Probable-Pathogenic
Disease	Chronic lymphocytic leukemia Myelodysplastic syndrome Pancreatic adenocarcinoma Neoplasm of breast Acute myeloid leukemia Medulloblastoma Renal cell carcinoma
Variation	info
Gene	SF3B2
CLNDBN	Chronic lymphocytic leukemia Myelodysplastic syndrome Pancreatic adenocarcinoma Neoplasm of breast Acute myeloid leukemia Medulloblastoma Renal cell carcinoma
Reversed	0
HGVS	NC_000011.9:g.65830884A>G
CLNSRC
CLNACC	RCV000423295.1, RCV000424642.1, RCV000425258.1, RCV000433609.1, RCV000436411.1, RCV000444087.1, RCV000444245.1,