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rs587781407

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781407(A;G)
Make rs587781407(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position86923592
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs587781407
ebirs587781407
HLIrs587781407
Exacrs587781407
Varsomers587781407
Maprs587781407
PheGenIrs587781407
hapmaprs587781407
1000 genomesrs587781407
hgdprs587781407
ensemblrs587781407
gopubmedrs587781407
geneviewrs587781407
scholarrs587781407
googlers587781407
pharmgkbrs587781407
gwascentralrs587781407
openSNPrs587781407
23andMers587781407
23andMe allrs587781407
SNP Nexus

SNPshotrs587781407
SNPdbers587781407
MSV3drs587781407
GWAS Ctlgrs587781407
Max Magnitude0
ClinVar
Risk rs587781407(G;G)
Alt rs587781407(G;G)
Reference rs587781407(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BMPR1A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.88683349A>G
CLNSRC
CLNACC RCV000129262.2,