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rs786202082

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202082(C;G)
Make rs786202082(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position7673793
GeneTP53
is asnp
is mentioned by
dbSNPrs786202082
ebirs786202082
HLIrs786202082
Exacrs786202082
Varsomers786202082
Maprs786202082
PheGenIrs786202082
hapmaprs786202082
1000 genomesrs786202082
hgdprs786202082
ensemblrs786202082
gopubmedrs786202082
geneviewrs786202082
scholarrs786202082
googlers786202082
pharmgkbrs786202082
gwascentralrs786202082
openSNPrs786202082
23andMers786202082
23andMe allrs786202082
SNP Nexus

SNPshotrs786202082
SNPdbers786202082
MSV3drs786202082
GWAS Ctlgrs786202082
Max Magnitude0
ClinVar
Risk rs786202082(A,G;A,G)
Alt rs786202082(A,G;A,G)
Reference rs786202082(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000017.10:g.7577111G>C; NC_000017.10:g.7577111G>T
CLNSRC
CLNACC RCV000164718.1, RCV000223364.1, RCV000236401.1,