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rs876660079

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660079(A;A)
Make rs876660079(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position51048733
GeneSMAD4
is asnp
is mentioned by
dbSNPrs876660079
ebirs876660079
HLIrs876660079
Exacrs876660079
Varsomers876660079
Maprs876660079
PheGenIrs876660079
hapmaprs876660079
1000 genomesrs876660079
hgdprs876660079
ensemblrs876660079
gopubmedrs876660079
geneviewrs876660079
scholarrs876660079
googlers876660079
pharmgkbrs876660079
gwascentralrs876660079
openSNPrs876660079
23andMers876660079
23andMe allrs876660079
SNP Nexus

SNPshotrs876660079
SNPdbers876660079
MSV3drs876660079
GWAS Ctlgrs876660079
Max Magnitude0
ClinVar
Risk rs876660079(A;A)
Alt rs876660079(A;A)
Reference rs876660079(G;G)
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.48575103G>A
CLNSRC
CLNACC RCV000217432.1,