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rs137852745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852745(A;G)
Make rs137852745(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position202552756
GeneBMPR2
is asnp
is mentioned by
dbSNPrs137852745
ebirs137852745
HLIrs137852745
Exacrs137852745
Varsomers137852745
Maprs137852745
PheGenIrs137852745
hapmaprs137852745
1000 genomesrs137852745
hgdprs137852745
ensemblrs137852745
gopubmedrs137852745
geneviewrs137852745
scholarrs137852745
googlers137852745
pharmgkbrs137852745
gwascentralrs137852745
openSNPrs137852745
23andMers137852745
23andMe allrs137852745
SNP Nexus

SNPshotrs137852745
SNPdbers137852745
MSV3drs137852745
GWAS Ctlgrs137852745
Max Magnitude0
OMIM600799
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852745(G;G)
Alt rs137852745(G;G)
Reference rs137852745(A;A)
Significance Pathogenic
Disease Primary pulmonary hypertension
Variation info
Gene BMPR2
CLNDBN Primary pulmonary hypertension
Reversed 0
HGVS NC_000002.11:g.203417479A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009346.2,