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rs876661106

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661106(A;T)
Make rs876661106(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68801843
GeneCDH1
is asnp
is mentioned by
dbSNPrs876661106
ebirs876661106
HLIrs876661106
Exacrs876661106
Varsomers876661106
Maprs876661106
PheGenIrs876661106
hapmaprs876661106
1000 genomesrs876661106
hgdprs876661106
ensemblrs876661106
gopubmedrs876661106
geneviewrs876661106
scholarrs876661106
googlers876661106
pharmgkbrs876661106
gwascentralrs876661106
openSNPrs876661106
23andMers876661106
23andMe allrs876661106
SNP Nexus

SNPshotrs876661106
SNPdbers876661106
MSV3drs876661106
GWAS Ctlgrs876661106
Max Magnitude0
ClinVar
Risk rs876661106(G,T;G,T)
Alt rs876661106(G,T;G,T)
Reference rs876661106(A;A)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene CDH1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000016.9:g.68835746A>G; NC_000016.9:g.68835746A>T
CLNSRC
CLNACC RCV000217135.1, RCV000220040.1,