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rs374250186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs374250186(A;A)
Make rs374250186(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position197402636
GeneSF3B1
is asnp
is mentioned by
dbSNPrs374250186
dbSNP (classic)rs374250186
ClinGenrs374250186
ebirs374250186
HLIrs374250186
Exacrs374250186
Gnomadrs374250186
Varsomers374250186
LitVarrs374250186
Maprs374250186
PheGenIrs374250186
Biobankrs374250186
1000 genomesrs374250186
hgdprs374250186
ensemblrs374250186
geneviewrs374250186
scholarrs374250186
googlers374250186
pharmgkbrs374250186
gwascentralrs374250186
openSNPrs374250186
23andMers374250186
SNPshotrs374250186
SNPdbers374250186
MSV3drs374250186
GWAS Ctlgrs374250186
Max Magnitude0
ClinVar
Risk rs374250186(A;A) rs374250186(C;C) rs374250186(G;G)
Alt rs374250186(A;A) rs374250186(C;C) rs374250186(G;G)
Reference Rs374250186(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene SF3B1
CLNDBN Acute myeloid leukemia
Reversed 0
HGVS NC_000002.11:g.198267360T>C; NC_000002.11:g.198267360T>G
CLNSRC
CLNACC RCV000428735.1, RCV000438980.1,