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rs797046041

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797046041(C;G)
Make rs797046041(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position1282578
GeneTERT
is asnp
is mentioned by
dbSNPrs797046041
ebirs797046041
HLIrs797046041
Exacrs797046041
Varsomers797046041
Maprs797046041
PheGenIrs797046041
hapmaprs797046041
1000 genomesrs797046041
hgdprs797046041
ensemblrs797046041
gopubmedrs797046041
geneviewrs797046041
scholarrs797046041
googlers797046041
pharmgkbrs797046041
gwascentralrs797046041
openSNPrs797046041
23andMers797046041
23andMe allrs797046041
SNP Nexus

SNPshotrs797046041
SNPdbers797046041
MSV3drs797046041
GWAS Ctlgrs797046041
Max Magnitude0
ClinVar
Risk rs797046041(G;G)
Alt rs797046041(G;G)
Reference rs797046041(C;C)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene TERT
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000005.9:g.1282693G>C
CLNSRC
CLNACC RCV000193118.1,