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rs876660150

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660150(-;-)
Make rs876660150(-;TT)
Make rs876660150(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position51078394
GeneSMAD4
is asnp
is mentioned by
dbSNPrs876660150
ebirs876660150
HLIrs876660150
Exacrs876660150
Varsomers876660150
Maprs876660150
PheGenIrs876660150
hapmaprs876660150
1000 genomesrs876660150
hgdprs876660150
ensemblrs876660150
gopubmedrs876660150
geneviewrs876660150
scholarrs876660150
googlers876660150
pharmgkbrs876660150
gwascentralrs876660150
openSNPrs876660150
23andMers876660150
23andMe allrs876660150
SNP Nexus

SNPshotrs876660150
SNPdbers876660150
MSV3drs876660150
GWAS Ctlgrs876660150
Max Magnitude0
ClinVar
Risk rs876660150(TT;TT)
Alt rs876660150(TT;TT)
Reference rs876660150(;)
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.48604763_48604764dupTT
CLNSRC
CLNACC RCV000220401.1,