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rs876658891

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658891(G;G)
Make rs876658891(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position86892205
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs876658891
ebirs876658891
HLIrs876658891
Exacrs876658891
Varsomers876658891
Maprs876658891
PheGenIrs876658891
hapmaprs876658891
1000 genomesrs876658891
hgdprs876658891
ensemblrs876658891
gopubmedrs876658891
geneviewrs876658891
scholarrs876658891
googlers876658891
pharmgkbrs876658891
gwascentralrs876658891
openSNPrs876658891
23andMers876658891
23andMe allrs876658891
SNP Nexus

SNPshotrs876658891
SNPdbers876658891
MSV3drs876658891
GWAS Ctlgrs876658891
Max Magnitude0
ClinVar
Risk rs876658891(G;G)
Alt rs876658891(G;G)
Reference rs876658891(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BMPR1A
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.88651962T>G
CLNSRC
CLNACC RCV000218016.1,