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rs62619935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62619935(C;T)
Make rs62619935(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position112792446
GeneAPC
is asnp
is mentioned by
dbSNPrs62619935
ebirs62619935
HLIrs62619935
Exacrs62619935
Varsomers62619935
Maprs62619935
PheGenIrs62619935
hapmaprs62619935
1000 genomesrs62619935
hgdprs62619935
ensemblrs62619935
gopubmedrs62619935
geneviewrs62619935
scholarrs62619935
googlers62619935
pharmgkbrs62619935
gwascentralrs62619935
openSNPrs62619935
23andMers62619935
23andMe allrs62619935
SNP Nexus

SNPshotrs62619935
SNPdbers62619935
MSV3drs62619935
GWAS Ctlgrs62619935
Max Magnitude0


ClinVar
Risk rs62619935(G,T;G,T)
Alt rs62619935(G,T;G,T)
Reference rs62619935(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112128143C>G; NC_000005.9:g.112128143C>T
CLNSRC Ambry Genetics ClinVar GeneDx
CLNACC RCV000130641.2, RCV000115111.3, RCV000223521.1,