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rs876659098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACACT;ACACT) 0 common in clinvar
Make rs876659098(ACACT;CAGGTCAGGACATCCA)
Make rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7674193
GeneTP53
is asnp
is mentioned by
dbSNPrs876659098
dbSNP (old)rs876659098
ClinGenrs876659098
ebirs876659098
HLIrs876659098
Exacrs876659098
Gnomadrs876659098
Varsomers876659098
Maprs876659098
PheGenIrs876659098
Biobankrs876659098
1000 genomesrs876659098
hgdprs876659098
ensemblrs876659098
gopubmedrs876659098
geneviewrs876659098
scholarrs876659098
googlers876659098
pharmgkbrs876659098
gwascentralrs876659098
openSNPrs876659098
23andMers876659098
23andMe allrs876659098
SNP Nexus

SNPshotrs876659098
SNPdbers876659098
MSV3drs876659098
GWAS Ctlgrs876659098
Max Magnitude0
ClinVar
Risk rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
Alt rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
Reference Rs876659098(ACACT;ACACT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577511_7577515delAGTGTinsTGGATGTCCTGACCTG
CLNSRC
CLNACC RCV000219279.1,