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rs876658515

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658515(C;T)
Make rs876658515(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position86923471
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs876658515
ebirs876658515
HLIrs876658515
Exacrs876658515
Varsomers876658515
Maprs876658515
PheGenIrs876658515
hapmaprs876658515
1000 genomesrs876658515
hgdprs876658515
ensemblrs876658515
gopubmedrs876658515
geneviewrs876658515
scholarrs876658515
googlers876658515
pharmgkbrs876658515
gwascentralrs876658515
openSNPrs876658515
23andMers876658515
23andMe allrs876658515
SNP Nexus

SNPshotrs876658515
SNPdbers876658515
MSV3drs876658515
GWAS Ctlgrs876658515
Max Magnitude0
ClinVar
Risk rs876658515(T;T)
Alt rs876658515(T;T)
Reference rs876658515(C;C)
Significance Probable-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.88683228C>T
CLNSRC
CLNACC RCV000219866.1,