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

rs786202785

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202785(A;A)
Make rs786202785(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68828281
GeneCDH1
is asnp
is mentioned by
dbSNPrs786202785
ebirs786202785
HLIrs786202785
Exacrs786202785
Varsomers786202785
Maprs786202785
PheGenIrs786202785
hapmaprs786202785
1000 genomesrs786202785
hgdprs786202785
ensemblrs786202785
gopubmedrs786202785
geneviewrs786202785
scholarrs786202785
googlers786202785
pharmgkbrs786202785
gwascentralrs786202785
openSNPrs786202785
23andMers786202785
23andMe allrs786202785
SNP Nexus

SNPshotrs786202785
SNPdbers786202785
MSV3drs786202785
GWAS Ctlgrs786202785
Max Magnitude0
ClinVar
Risk rs786202785(A;A)
Alt rs786202785(A;A)
Reference rs786202785(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68862184G>A
CLNSRC
CLNACC RCV000165772.1,