rs377023736
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs377023736(C;G) |
Make rs377023736(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 197402635 |
Gene | SF3B1 |
is a | snp |
is | mentioned by |
dbSNP | rs377023736 |
dbSNP (classic) | rs377023736 |
ClinGen | rs377023736 |
ebi | rs377023736 |
HLI | rs377023736 |
Exac | rs377023736 |
Gnomad | rs377023736 |
Varsome | rs377023736 |
LitVar | rs377023736 |
Map | rs377023736 |
PheGenI | rs377023736 |
Biobank | rs377023736 |
1000 genomes | rs377023736 |
hgdp | rs377023736 |
ensembl | rs377023736 |
geneview | rs377023736 |
scholar | rs377023736 |
rs377023736 | |
pharmgkb | rs377023736 |
gwascentral | rs377023736 |
openSNP | rs377023736 |
23andMe | rs377023736 |
SNPshot | rs377023736 |
SNPdbe | rs377023736 |
MSV3d | rs377023736 |
GWAS Ctlg | rs377023736 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377023736(A;A) rs377023736(G;G) |
Alt | rs377023736(A;A) rs377023736(G;G) |
Reference | Rs377023736(C;C) |
Significance | Pathogenic |
Disease | Myelodysplastic syndrome progressed to acute myeloid leukemia Myelodysplastic syndrome Acute myeloid leukemia |
Variation | info |
Gene | SF3B1 |
CLNDBN | Myelodysplastic syndrome progressed to acute myeloid leukemia Myelodysplastic syndrome Acute myeloid leukemia |
Reversed | 0 |
HGVS | NC_000002.11:g.198267359C>A; NC_000002.11:g.198267359C>G |
CLNSRC | |
CLNACC | RCV000203465.1, RCV000431140.1, RCV000441310.1, RCV000420231.1, |