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rs786203576

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar


Make rs786203576(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68738308
GeneCDH1
is asnp
is mentioned by
dbSNPrs786203576
ebirs786203576
HLIrs786203576
Exacrs786203576
Varsomers786203576
Maprs786203576
PheGenIrs786203576
hapmaprs786203576
1000 genomesrs786203576
hgdprs786203576
ensemblrs786203576
gopubmedrs786203576
geneviewrs786203576
scholarrs786203576
googlers786203576
pharmgkbrs786203576
gwascentralrs786203576
openSNPrs786203576
23andMers786203576
23andMe allrs786203576
SNP Nexus

SNPshotrs786203576
SNPdbers786203576
MSV3drs786203576
GWAS Ctlgrs786203576
Max Magnitude0
ClinVar
Risk rs786203576(A;A)
Alt rs786203576(A;A)
Reference rs786203576(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68772211G>A
CLNSRC
CLNACC RCV000166954.1,