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rs587782388

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782388(A;A)
Make rs587782388(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position86899831
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs587782388
ebirs587782388
HLIrs587782388
Exacrs587782388
Varsomers587782388
Maprs587782388
PheGenIrs587782388
hapmaprs587782388
1000 genomesrs587782388
hgdprs587782388
ensemblrs587782388
gopubmedrs587782388
geneviewrs587782388
scholarrs587782388
googlers587782388
pharmgkbrs587782388
gwascentralrs587782388
openSNPrs587782388
23andMers587782388
23andMe allrs587782388
SNP Nexus

SNPshotrs587782388
SNPdbers587782388
MSV3drs587782388
GWAS Ctlgrs587782388
Max Magnitude0
ClinVar
Risk rs587782388(A;A)
Alt rs587782388(A;A)
Reference rs587782388(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BMPR1A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.88659588G>A
CLNSRC
CLNACC RCV000131396.2,