Have questions? Visit https://www.reddit.com/r/SNPedia

rs786201058

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 5 Hereditary cancer-predisposing syndrome; gastric cancer related?
Make rs786201058(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68738324
GeneCDH1
is asnp
is mentioned by
dbSNPrs786201058
ebirs786201058
HLIrs786201058
Exacrs786201058
Varsomers786201058
Maprs786201058
PheGenIrs786201058
hapmaprs786201058
1000 genomesrs786201058
hgdprs786201058
ensemblrs786201058
gopubmedrs786201058
geneviewrs786201058
scholarrs786201058
googlers786201058
pharmgkbrs786201058
gwascentralrs786201058
openSNPrs786201058
23andMers786201058
23andMe allrs786201058
SNP Nexus

SNPshotrs786201058
SNPdbers786201058
MSV3drs786201058
GWAS Ctlgrs786201058
Max Magnitude5
ClinVar
Risk rs786201058(T;T)
Alt rs786201058(T;T)
Reference rs786201058(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68772227G>C; NC_000016.9:g.68772227G>T
CLNSRC
CLNACC RCV000223374.1, RCV000162463.1,