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rs869312758

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312758(C;C)
Make rs869312758(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position86876021
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs869312758
ebirs869312758
HLIrs869312758
Exacrs869312758
Varsomers869312758
Maprs869312758
PheGenIrs869312758
hapmaprs869312758
1000 genomesrs869312758
hgdprs869312758
ensemblrs869312758
gopubmedrs869312758
geneviewrs869312758
scholarrs869312758
googlers869312758
pharmgkbrs869312758
gwascentralrs869312758
openSNPrs869312758
23andMers869312758
23andMe allrs869312758
SNP Nexus

SNPshotrs869312758
SNPdbers869312758
MSV3drs869312758
GWAS Ctlgrs869312758
Max Magnitude0
ClinVar
Risk rs869312758(C;C)
Alt rs869312758(C;C)
Reference rs869312758(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BMPR1A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.88635778G>C
CLNSRC
CLNACC RCV000210125.1,