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rs796065341

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796065341(G;G)
Make rs796065341(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136504916
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs796065341
ebirs796065341
HLIrs796065341
Exacrs796065341
Varsomers796065341
Maprs796065341
PheGenIrs796065341
hapmaprs796065341
1000 genomesrs796065341
hgdprs796065341
ensemblrs796065341
gopubmedrs796065341
geneviewrs796065341
scholarrs796065341
googlers796065341
pharmgkbrs796065341
gwascentralrs796065341
openSNPrs796065341
23andMers796065341
23andMe allrs796065341
SNP Nexus

SNPshotrs796065341
SNPdbers796065341
MSV3drs796065341
GWAS Ctlgrs796065341
Max Magnitude0
ClinVar
Risk rs796065341(G;G)
Alt rs796065341(G;G)
Reference rs796065341(T;T)
Significance Pathogenic
Disease Early T cell progenitor acute lymphoblastic leukemia
Variation info
Gene NOTCH1
CLNDBN Early T cell progenitor acute lymphoblastic leukemia
Reversed 1
HGVS NC_000009.11:g.139399368A>C
CLNSRC
CLNACC RCV000190416.1,