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rs876659446

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659446(-;-)
Make rs876659446(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68812264
GeneCDH1
is asnp
is mentioned by
dbSNPrs876659446
ebirs876659446
HLIrs876659446
Exacrs876659446
Varsomers876659446
Maprs876659446
PheGenIrs876659446
hapmaprs876659446
1000 genomesrs876659446
hgdprs876659446
ensemblrs876659446
gopubmedrs876659446
geneviewrs876659446
scholarrs876659446
googlers876659446
pharmgkbrs876659446
gwascentralrs876659446
openSNPrs876659446
23andMers876659446
23andMe allrs876659446
SNP Nexus

SNPshotrs876659446
SNPdbers876659446
MSV3drs876659446
GWAS Ctlgrs876659446
Max Magnitude0
ClinVar
Risk rs876659446(;)
Alt rs876659446(;)
Reference rs876659446(G;G)
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.68846167delG
CLNSRC
CLNACC RCV000218840.1,