Have questions? Visit https://www.reddit.com/r/SNPedia

rs371409680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371409680(C;T)
Make rs371409680(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position7673772
GeneTP53
is asnp
is mentioned by
dbSNPrs371409680
ebirs371409680
HLIrs371409680
Exacrs371409680
Varsomers371409680
Maprs371409680
PheGenIrs371409680
hapmaprs371409680
1000 genomesrs371409680
hgdprs371409680
ensemblrs371409680
gopubmedrs371409680
geneviewrs371409680
scholarrs371409680
googlers371409680
pharmgkbrs371409680
gwascentralrs371409680
openSNPrs371409680
23andMers371409680
23andMe allrs371409680
SNP Nexus

SNPshotrs371409680
SNPdbers371409680
MSV3drs371409680
GWAS Ctlgrs371409680
Max Magnitude0
ClinVar
Risk rs371409680(T;T)
Alt rs371409680(T;T)
Reference rs371409680(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Astrocytoma not provided
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Astrocytoma not provided
Reversed 0
HGVS NC_000017.10:g.7577090C>T
CLNSRC Ambry Genetics ClinVar University of Washington
CLNACC RCV000131388.4, RCV000148904.2, RCV000213060.1,