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rs876660548

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660548(A;A)
Make rs876660548(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7676096
GeneTP53
is asnp
is mentioned by
dbSNPrs876660548
ebirs876660548
HLIrs876660548
Exacrs876660548
Varsomers876660548
Maprs876660548
PheGenIrs876660548
hapmaprs876660548
1000 genomesrs876660548
hgdprs876660548
ensemblrs876660548
gopubmedrs876660548
geneviewrs876660548
scholarrs876660548
googlers876660548
pharmgkbrs876660548
gwascentralrs876660548
openSNPrs876660548
23andMers876660548
23andMe allrs876660548
SNP Nexus

SNPshotrs876660548
SNPdbers876660548
MSV3drs876660548
GWAS Ctlgrs876660548
Max Magnitude0
ClinVar
Risk rs876660548(A;A)
Alt rs876660548(A;A)
Reference rs876660548(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Li-Fraumeni syndrome
Reversed 1
HGVS NC_000017.10:g.7579414C>T
CLNSRC
CLNACC RCV000220815.1, RCV000233967.1,