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rs1061157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1061157(A;A)
Make rs1061157(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position202556476
GeneBMPR2
is asnp
is mentioned by
dbSNPrs1061157
ebirs1061157
HLIrs1061157
Exacrs1061157
Varsomers1061157
Maprs1061157
PheGenIrs1061157
hapmaprs1061157
1000 genomesrs1061157
hgdprs1061157
ensemblrs1061157
gopubmedrs1061157
geneviewrs1061157
scholarrs1061157
googlers1061157
pharmgkbrs1061157
gwascentralrs1061157
openSNPrs1061157
23andMers1061157
23andMe allrs1061157
SNP Nexus

SNPshotrs1061157
SNPdbers1061157
MSV3drs1061157
GWAS Ctlgrs1061157
GMAF0.0877
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 23098893] 5'UTR Repeat Polymorphisms of the BMPR2 gene in Children with Pulmonary Hypertension associated with Congenital Heart Disease


[PMID 21311592OA-icon.png] Genetic and evolutionary analyses of the human bone morphogenetic protein receptor 2 (BMPR2) in the pathophysiology of obesity.


ClinVar
Risk rs1061157(A;A)
Alt rs1061157(A;A)
Reference rs1061157(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene BMPR2
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.203421199G>A
CLNSRC ClinVar GeneDx
CLNACC RCV000150194.3,