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rs876661120

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661120(C;C)
Make rs876661120(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68823628
GeneCDH1
is asnp
is mentioned by
dbSNPrs876661120
ebirs876661120
HLIrs876661120
Exacrs876661120
Varsomers876661120
Maprs876661120
PheGenIrs876661120
hapmaprs876661120
1000 genomesrs876661120
hgdprs876661120
ensemblrs876661120
gopubmedrs876661120
geneviewrs876661120
scholarrs876661120
googlers876661120
pharmgkbrs876661120
gwascentralrs876661120
openSNPrs876661120
23andMers876661120
23andMe allrs876661120
SNP Nexus

SNPshotrs876661120
SNPdbers876661120
MSV3drs876661120
GWAS Ctlgrs876661120
Max Magnitude0
ClinVar
Risk rs876661120(C;C)
Alt rs876661120(C;C)
Reference rs876661120(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CDH1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.68857531T>C
CLNSRC
CLNACC RCV000215849.1,