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rs1057519959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519959(A;C)
Make rs1057519959(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position66063028
GeneSF3B2
is asnp
is mentioned by
dbSNPrs1057519959
dbSNP (classic)rs1057519959
ClinGenrs1057519959
ebirs1057519959
HLIrs1057519959
Exacrs1057519959
Gnomadrs1057519959
Varsomers1057519959
LitVarrs1057519959
Maprs1057519959
PheGenIrs1057519959
Biobankrs1057519959
1000 genomesrs1057519959
hgdprs1057519959
ensemblrs1057519959
geneviewrs1057519959
scholarrs1057519959
googlers1057519959
pharmgkbrs1057519959
gwascentralrs1057519959
openSNPrs1057519959
23andMers1057519959
23andMe allrs1057519959
SNPshotrs1057519959
SNPdbers1057519959
MSV3drs1057519959
GWAS Ctlgrs1057519959
Max Magnitude0
ClinVar
Risk rs1057519959(C;C)
Alt rs1057519959(C;C)
Reference Rs1057519959(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Chronic lymphocytic leukemia Hepatocellular carcinoma Neoplasm of breast
Variation info
Gene SF3B2
CLNDBN Malignant melanoma of skin Chronic lymphocytic leukemia Hepatocellular carcinoma Neoplasm of breast
Reversed 0
HGVS NC_000011.9:g.65830499A>C
CLNSRC
CLNACC RCV000423874.1, RCV000428737.1, RCV000434162.1, RCV000438957.1,