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rs786203089

From SNPedia

Orientationplus
Geno Mag Summary
(GGTAAG;GGTAAG) 0 common in clinvar
Make rs786203089(-;-)
Make rs786203089(-;TAAGGG)
Make rs786203089(TAAGGG;TAAGGG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position68819427
GeneCDH1
is asnp
is mentioned by
dbSNPrs786203089
ebirs786203089
HLIrs786203089
Exacrs786203089
Varsomers786203089
Maprs786203089
PheGenIrs786203089
hapmaprs786203089
1000 genomesrs786203089
hgdprs786203089
ensemblrs786203089
gopubmedrs786203089
geneviewrs786203089
scholarrs786203089
googlers786203089
pharmgkbrs786203089
gwascentralrs786203089
openSNPrs786203089
23andMers786203089
23andMe allrs786203089
SNP Nexus

SNPshotrs786203089
SNPdbers786203089
MSV3drs786203089
GWAS Ctlgrs786203089
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs786203089(GGTAAG;GGTAAG)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68853330_68853335delTAAGGG
CLNSRC
CLNACC RCV000166240.1,