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rs730881663

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881663(A;A)
Make rs730881663(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position68810216
GeneCDH1
is asnp
is mentioned by
dbSNPrs730881663
ebirs730881663
HLIrs730881663
Exacrs730881663
Varsomers730881663
Maprs730881663
PheGenIrs730881663
hapmaprs730881663
1000 genomesrs730881663
hgdprs730881663
ensemblrs730881663
gopubmedrs730881663
geneviewrs730881663
scholarrs730881663
googlers730881663
pharmgkbrs730881663
gwascentralrs730881663
openSNPrs730881663
23andMers730881663
23andMe allrs730881663
SNP Nexus

SNPshotrs730881663
SNPdbers730881663
MSV3drs730881663
GWAS Ctlgrs730881663
Max Magnitude0
ClinVar
Risk rs730881663(A;A)
Alt rs730881663(A;A)
Reference rs730881663(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDH1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.68844119C>A
CLNSRC
CLNACC RCV000160385.2,