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rs876659208

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome16
Position68815670
GeneCDH1
is asnp
is mentioned by
dbSNPrs876659208
dbSNP (classic)rs876659208
ClinGenrs876659208
ebirs876659208
HLIrs876659208
Exacrs876659208
Gnomadrs876659208
Varsomers876659208
LitVarrs876659208
Maprs876659208
PheGenIrs876659208
Biobankrs876659208
1000 genomesrs876659208
hgdprs876659208
ensemblrs876659208
geneviewrs876659208
scholarrs876659208
googlers876659208
pharmgkbrs876659208
gwascentralrs876659208
openSNPrs876659208
23andMers876659208
SNPshotrs876659208
SNPdbers876659208
MSV3drs876659208
GWAS Ctlgrs876659208
Max Magnitude0
ClinVar
Risk rs876659208(-;-)
Alt rs876659208(-;-)
Reference Rs876659208(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.68849573_68849574delAG
CLNSRC
CLNACC RCV000213871.2,