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rs869025366

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025366(C;T)
Make rs869025366(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position202513739
GeneBMPR2
is asnp
is mentioned by
dbSNPrs869025366
ebirs869025366
HLIrs869025366
Exacrs869025366
Varsomers869025366
Maprs869025366
PheGenIrs869025366
hapmaprs869025366
1000 genomesrs869025366
hgdprs869025366
ensemblrs869025366
gopubmedrs869025366
geneviewrs869025366
scholarrs869025366
googlers869025366
pharmgkbrs869025366
gwascentralrs869025366
openSNPrs869025366
23andMers869025366
23andMe allrs869025366
SNP Nexus

SNPshotrs869025366
SNPdbers869025366
MSV3drs869025366
GWAS Ctlgrs869025366
Max Magnitude0
ClinVar
Risk rs869025366(T;T)
Alt rs869025366(T;T)
Reference rs869025366(C;C)
Significance Pathogenic
Disease Primary pulmonary hypertension
Variation info
Gene BMPR2
CLNDBN Primary pulmonary hypertension
Reversed 0
HGVS NC_000002.11:g.203378462C>T
CLNSRC
CLNACC RCV000208112.1,