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rs869025367

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025367(C;C)
Make rs869025367(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position202532732
GeneBMPR2
is asnp
is mentioned by
dbSNPrs869025367
ebirs869025367
HLIrs869025367
Exacrs869025367
Varsomers869025367
Maprs869025367
PheGenIrs869025367
hapmaprs869025367
1000 genomesrs869025367
hgdprs869025367
ensemblrs869025367
gopubmedrs869025367
geneviewrs869025367
scholarrs869025367
googlers869025367
pharmgkbrs869025367
gwascentralrs869025367
openSNPrs869025367
23andMers869025367
23andMe allrs869025367
SNP Nexus

SNPshotrs869025367
SNPdbers869025367
MSV3drs869025367
GWAS Ctlgrs869025367
Max Magnitude0
ClinVar
Risk rs869025367(C;C)
Alt rs869025367(C;C)
Reference rs869025367(G;G)
Significance Probable-Pathogenic
Disease Primary pulmonary hypertension
Variation info
Gene BMPR2
CLNDBN Primary pulmonary hypertension
Reversed 0
HGVS NC_000002.11:g.203397455G>C
CLNSRC
CLNACC RCV000208298.1,