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rs587782494

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782494(C;T)
Make rs587782494(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position86899815
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs587782494
ebirs587782494
HLIrs587782494
Exacrs587782494
Varsomers587782494
Maprs587782494
PheGenIrs587782494
hapmaprs587782494
1000 genomesrs587782494
hgdprs587782494
ensemblrs587782494
gopubmedrs587782494
geneviewrs587782494
scholarrs587782494
googlers587782494
pharmgkbrs587782494
gwascentralrs587782494
openSNPrs587782494
23andMers587782494
23andMe allrs587782494
SNP Nexus

SNPshotrs587782494
SNPdbers587782494
MSV3drs587782494
GWAS Ctlgrs587782494
Max Magnitude0
ClinVar
Risk rs587782494(T;T)
Alt rs587782494(T;T)
Reference rs587782494(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BMPR1A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.88659572C>T
CLNSRC
CLNACC RCV000131622.2,