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rs11540654

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11540654(C;C)
Make rs11540654(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7676040
GeneTP53
is asnp
is mentioned by
dbSNPrs11540654
ebirs11540654
HLIrs11540654
Exacrs11540654
Varsomers11540654
Maprs11540654
PheGenIrs11540654
hapmaprs11540654
1000 genomesrs11540654
hgdprs11540654
ensemblrs11540654
gopubmedrs11540654
geneviewrs11540654
scholarrs11540654
googlers11540654
pharmgkbrs11540654
gwascentralrs11540654
openSNPrs11540654
23andMers11540654
23andMe allrs11540654
SNP Nexus

SNPshotrs11540654
SNPdbers11540654
MSV3drs11540654
GWAS Ctlgrs11540654
Max Magnitude0
ClinVar
Risk rs11540654(A,C,T;A,C,T)
Alt rs11540654(A,C,T;A,C,T)
Reference rs11540654(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Li-Fraumeni syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.7579358C>G; NC_000017.10:g.7579358C>T
CLNSRC
CLNACC RCV000222678.1, RCV000231991.1, RCV000115719.5, RCV000122182.1, RCV000228299.1,