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rs876660556

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660556(A;A)
Make rs876660556(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position51065555
GeneSMAD4
is asnp
is mentioned by
dbSNPrs876660556
ebirs876660556
HLIrs876660556
Exacrs876660556
Varsomers876660556
Maprs876660556
PheGenIrs876660556
hapmaprs876660556
1000 genomesrs876660556
hgdprs876660556
ensemblrs876660556
gopubmedrs876660556
geneviewrs876660556
scholarrs876660556
googlers876660556
pharmgkbrs876660556
gwascentralrs876660556
openSNPrs876660556
23andMers876660556
23andMe allrs876660556
SNP Nexus

SNPshotrs876660556
SNPdbers876660556
MSV3drs876660556
GWAS Ctlgrs876660556
Max Magnitude0
ClinVar
Risk rs876660556(A;A)
Alt rs876660556(A;A)
Reference rs876660556(G;G)
Significance Probable-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.48591925G>A
CLNSRC
CLNACC RCV000219161.1,