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rs559063155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs559063155(A;A)
Make rs559063155(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position197402110
GeneSF3B1
is asnp
is mentioned by
dbSNPrs559063155
dbSNP (classic)rs559063155
ClinGenrs559063155
ebirs559063155
HLIrs559063155
Exacrs559063155
Gnomadrs559063155
Varsomers559063155
LitVarrs559063155
Maprs559063155
PheGenIrs559063155
Biobankrs559063155
1000 genomesrs559063155
hgdprs559063155
ensemblrs559063155
geneviewrs559063155
scholarrs559063155
googlers559063155
pharmgkbrs559063155
gwascentralrs559063155
openSNPrs559063155
23andMers559063155
SNPshotrs559063155
SNPdbers559063155
MSV3drs559063155
GWAS Ctlgrs559063155
Max Magnitude0
ClinVar
Risk rs559063155(A;A) rs559063155(C;C) rs559063155(G;G)
Alt rs559063155(A;A) rs559063155(C;C) rs559063155(G;G)
Reference Rs559063155(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene SF3B1
CLNDBN Acute myeloid leukemia
Reversed 0
HGVS NC_000002.11:g.198266834T>A; NC_000002.11:g.198266834T>C; NC_000002.11:g.198266834T>G
CLNSRC
CLNACC RCV000424424.1, RCV000420863.1, RCV000435126.1,