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rs876658694

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658694(C;T)
Make rs876658694(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position51059892
GeneSMAD4
is asnp
is mentioned by
dbSNPrs876658694
ebirs876658694
HLIrs876658694
Exacrs876658694
Varsomers876658694
Maprs876658694
PheGenIrs876658694
hapmaprs876658694
1000 genomesrs876658694
hgdprs876658694
ensemblrs876658694
gopubmedrs876658694
geneviewrs876658694
scholarrs876658694
googlers876658694
pharmgkbrs876658694
gwascentralrs876658694
openSNPrs876658694
23andMers876658694
23andMe allrs876658694
SNP Nexus

SNPshotrs876658694
SNPdbers876658694
MSV3drs876658694
GWAS Ctlgrs876658694
Max Magnitude0
ClinVar
Risk rs876658694(T;T)
Alt rs876658694(T;T)
Reference rs876658694(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SMAD4
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000018.9:g.48586262C>T
CLNSRC
CLNACC RCV000215604.1,