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rs876661118

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661118(-;-)
Make rs876661118(-;C)
Make rs876661118(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68822068
GeneCDH1
is asnp
is mentioned by
dbSNPrs876661118
ebirs876661118
HLIrs876661118
Exacrs876661118
Varsomers876661118
Maprs876661118
PheGenIrs876661118
hapmaprs876661118
1000 genomesrs876661118
hgdprs876661118
ensemblrs876661118
gopubmedrs876661118
geneviewrs876661118
scholarrs876661118
googlers876661118
pharmgkbrs876661118
gwascentralrs876661118
openSNPrs876661118
23andMers876661118
23andMe allrs876661118
SNP Nexus

SNPshotrs876661118
SNPdbers876661118
MSV3drs876661118
GWAS Ctlgrs876661118
Max Magnitude0
ClinVar
Risk rs876661118(C;C)
Alt rs876661118(C;C)
Reference rs876661118(;)
Significance Pathogenic
Disease not provided
Variation info
Gene CDH1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.68855971dupC
CLNSRC
CLNACC RCV000222914.1,