Have questions? Visit https://www.reddit.com/r/SNPedia

rs876660712

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876660712(-;-)
Make rs876660712(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position51047199
GeneSMAD4
is asnp
is mentioned by
dbSNPrs876660712
ebirs876660712
HLIrs876660712
Exacrs876660712
Varsomers876660712
Maprs876660712
PheGenIrs876660712
hapmaprs876660712
1000 genomesrs876660712
hgdprs876660712
ensemblrs876660712
gopubmedrs876660712
geneviewrs876660712
scholarrs876660712
googlers876660712
pharmgkbrs876660712
gwascentralrs876660712
openSNPrs876660712
23andMers876660712
23andMe allrs876660712
SNP Nexus

SNPshotrs876660712
SNPdbers876660712
MSV3drs876660712
GWAS Ctlgrs876660712
Max Magnitude0
ClinVar
Risk rs876660712(;)
Alt rs876660712(;)
Reference rs876660712(A;A)
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.48573569delA
CLNSRC
CLNACC RCV000218475.1,