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rs28934571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in complete genomics
Make rs28934571(G;T)
Make rs28934571(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7674216
GeneTP53
is asnp
is mentioned by
dbSNPrs28934571
ebirs28934571
HLIrs28934571
Exacrs28934571
Varsomers28934571
Maprs28934571
PheGenIrs28934571
hapmaprs28934571
1000 genomesrs28934571
hgdprs28934571
ensemblrs28934571
gopubmedrs28934571
geneviewrs28934571
scholarrs28934571
googlers28934571
pharmgkbrs28934571
gwascentralrs28934571
openSNPrs28934571
23andMers28934571
23andMe allrs28934571
SNP Nexus

SNPshotrs28934571
SNPdbers28934571
MSV3drs28934571
GWAS Ctlgrs28934571
Max Magnitude0
OMIM191170
DescHEPATOCELLULAR CARCINOMA
Variant0006
Relatedalso
Neighborrs28934577
Distance23
Neighborrs11540652
Distance4


ClinVar
Risk rs28934571(T;T)
Alt rs28934571(T;T)
Reference rs28934571(G;G)
Significance Pathogenic
Disease Hepatocellular carcinoma Carcinoma of cervix
Variation info
Gene TP53
CLNDBN Hepatocellular carcinoma Carcinoma of cervix
Reversed 1
HGVS NC_000017.10:g.7577534C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013145.4, RCV000013146.4,