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rs755415626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs755415626(C;T)
Make rs755415626(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position197401887
GeneSF3B1
is asnp
is mentioned by
dbSNPrs755415626
dbSNP (classic)rs755415626
ClinGenrs755415626
ebirs755415626
HLIrs755415626
Exacrs755415626
Gnomadrs755415626
Varsomers755415626
LitVarrs755415626
Maprs755415626
PheGenIrs755415626
Biobankrs755415626
1000 genomesrs755415626
hgdprs755415626
ensemblrs755415626
geneviewrs755415626
scholarrs755415626
googlers755415626
pharmgkbrs755415626
gwascentralrs755415626
openSNPrs755415626
23andMers755415626
SNPshotrs755415626
SNPdbers755415626
MSV3drs755415626
GWAS Ctlgrs755415626
Max Magnitude0
ClinVar
Risk rs755415626(T;T)
Alt rs755415626(T;T)
Reference Rs755415626(C;C)
Significance Probable-Pathogenic
Disease Chronic lymphocytic leukemia Renal cell carcinoma
Variation info
Gene SF3B1
CLNDBN Chronic lymphocytic leukemia Renal cell carcinoma
Reversed 0
HGVS NC_000002.11:g.198266611C>T
CLNSRC
CLNACC RCV000417601.1, RCV000438761.1,