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rs754688962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs754688962(C;C)
Make rs754688962(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position197402637
GeneSF3B1
is asnp
is mentioned by
dbSNPrs754688962
dbSNP (classic)rs754688962
ClinGenrs754688962
ebirs754688962
HLIrs754688962
Exacrs754688962
Gnomadrs754688962
Varsomers754688962
LitVarrs754688962
Maprs754688962
PheGenIrs754688962
Biobankrs754688962
1000 genomesrs754688962
hgdprs754688962
ensemblrs754688962
geneviewrs754688962
scholarrs754688962
googlers754688962
pharmgkbrs754688962
gwascentralrs754688962
openSNPrs754688962
23andMers754688962
SNPshotrs754688962
SNPdbers754688962
MSV3drs754688962
GWAS Ctlgrs754688962
Max Magnitude0
ClinVar
Risk rs754688962(C;C) rs754688962(G;G)
Alt rs754688962(C;C) rs754688962(G;G)
Reference Rs754688962(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of breast Hepatocellular carcinoma Chronic lymphocytic leukemia Malignant melanoma of skin Acute myeloid leukemia
Variation info
Gene SF3B1
CLNDBN Neoplasm of breast Hepatocellular carcinoma Chronic lymphocytic leukemia Malignant melanoma of skin Acute myeloid leukemia
Reversed 0
HGVS NC_000002.11:g.198267361T>C; NC_000002.11:g.198267361T>G
CLNSRC
CLNACC RCV000421290.1, RCV000422376.1, RCV000431560.1, RCV000432266.1, RCV000440031.1, RCV000423955.1, RCV000433378.1, RCV000441810.1, RCV000445187.1,