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rs377023736

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377023736(C;G)
Make rs377023736(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position197402635
GeneSF3B1
is asnp
is mentioned by
dbSNPrs377023736
ebirs377023736
HLIrs377023736
Exacrs377023736
Varsomers377023736
Maprs377023736
PheGenIrs377023736
hapmaprs377023736
1000 genomesrs377023736
hgdprs377023736
ensemblrs377023736
gopubmedrs377023736
geneviewrs377023736
scholarrs377023736
googlers377023736
pharmgkbrs377023736
gwascentralrs377023736
openSNPrs377023736
23andMers377023736
23andMe allrs377023736
SNP Nexus

SNPshotrs377023736
SNPdbers377023736
MSV3drs377023736
GWAS Ctlgrs377023736
Max Magnitude0
ClinVar
Risk rs377023736(A,G;A,G)
Alt rs377023736(A,G;A,G)
Reference rs377023736(C;C)
Significance Pathogenic
Disease Myelodysplastic syndrome progressed to acute myeloid leukemia
Variation info
Gene SF3B1
CLNDBN Myelodysplastic syndrome progressed to acute myeloid leukemia
Reversed 0
HGVS NC_000002.11:g.198267359C>A
CLNSRC
CLNACC RCV000203465.1,