rs754688962
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs754688962(C;C) |
Make rs754688962(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 197402637 |
Gene | SF3B1 |
is a | snp |
is | mentioned by |
dbSNP | rs754688962 |
dbSNP (classic) | rs754688962 |
ClinGen | rs754688962 |
ebi | rs754688962 |
HLI | rs754688962 |
Exac | rs754688962 |
Gnomad | rs754688962 |
Varsome | rs754688962 |
LitVar | rs754688962 |
Map | rs754688962 |
PheGenI | rs754688962 |
Biobank | rs754688962 |
1000 genomes | rs754688962 |
hgdp | rs754688962 |
ensembl | rs754688962 |
geneview | rs754688962 |
scholar | rs754688962 |
rs754688962 | |
pharmgkb | rs754688962 |
gwascentral | rs754688962 |
openSNP | rs754688962 |
23andMe | rs754688962 |
SNPshot | rs754688962 |
SNPdbe | rs754688962 |
MSV3d | rs754688962 |
GWAS Ctlg | rs754688962 |
Max Magnitude | 0 |
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, |