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rs137852754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852754(A;A)
Make rs137852754(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position202514903
GeneBMPR2
is asnp
is mentioned by
dbSNPrs137852754
ebirs137852754
HLIrs137852754
Exacrs137852754
Varsomers137852754
Maprs137852754
PheGenIrs137852754
hapmaprs137852754
1000 genomesrs137852754
hgdprs137852754
ensemblrs137852754
gopubmedrs137852754
geneviewrs137852754
scholarrs137852754
googlers137852754
pharmgkbrs137852754
gwascentralrs137852754
openSNPrs137852754
23andMers137852754
23andMe allrs137852754
SNP Nexus

SNPshotrs137852754
SNPdbers137852754
MSV3drs137852754
GWAS Ctlgrs137852754
Max Magnitude0
OMIM600799
Desc
Variant0020
Relatedalso
ClinVar
Risk rs137852754(A;A)
Alt rs137852754(A;A)
Reference rs137852754(G;G)
Significance Pathogenic
Disease Pulmonary hypertension
Variation info
Gene BMPR2
CLNDBN Pulmonary hypertension, primary, fenfluramine-associated
Reversed 0
HGVS NC_000002.11:g.203379626G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009359.3,