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rs1057519960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519960(A;G)
Make rs1057519960(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position66063413
GeneSF3B2
is asnp
is mentioned by
dbSNPrs1057519960
dbSNP (old)rs1057519960
ClinGenrs1057519960
ebirs1057519960
HLIrs1057519960
Exacrs1057519960
Gnomadrs1057519960
Varsomers1057519960
Maprs1057519960
PheGenIrs1057519960
Biobankrs1057519960
1000 genomesrs1057519960
hgdprs1057519960
ensemblrs1057519960
gopubmedrs1057519960
geneviewrs1057519960
scholarrs1057519960
googlers1057519960
pharmgkbrs1057519960
gwascentralrs1057519960
openSNPrs1057519960
23andMers1057519960
23andMe allrs1057519960
SNPshotrs1057519960
SNPdbers1057519960
MSV3drs1057519960
GWAS Ctlgrs1057519960
Max Magnitude0
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,