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rs876660393

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660393(A;G)
Make rs876660393(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68829652
GeneCDH1
is asnp
is mentioned by
dbSNPrs876660393
ebirs876660393
HLIrs876660393
Exacrs876660393
Varsomers876660393
Maprs876660393
PheGenIrs876660393
hapmaprs876660393
1000 genomesrs876660393
hgdprs876660393
ensemblrs876660393
gopubmedrs876660393
geneviewrs876660393
scholarrs876660393
googlers876660393
pharmgkbrs876660393
gwascentralrs876660393
openSNPrs876660393
23andMers876660393
23andMe allrs876660393
SNP Nexus

SNPshotrs876660393
SNPdbers876660393
MSV3drs876660393
GWAS Ctlgrs876660393
Max Magnitude0
ClinVar
Risk rs876660393(G;G)
Alt rs876660393(G;G)
Reference rs876660393(A;A)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.68863555A>G
CLNSRC
CLNACC RCV000214820.1,