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rs137852741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852741(C;T)
Make rs137852741(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position202556360
GeneBMPR2
is asnp
is mentioned by
dbSNPrs137852741
ebirs137852741
HLIrs137852741
Exacrs137852741
Varsomers137852741
Maprs137852741
PheGenIrs137852741
hapmaprs137852741
1000 genomesrs137852741
hgdprs137852741
ensemblrs137852741
gopubmedrs137852741
geneviewrs137852741
scholarrs137852741
googlers137852741
pharmgkbrs137852741
gwascentralrs137852741
openSNPrs137852741
23andMers137852741
23andMe allrs137852741
SNP Nexus

SNPshotrs137852741
SNPdbers137852741
MSV3drs137852741
GWAS Ctlgrs137852741
Max Magnitude0
OMIM600799
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852741(G,T;G,T)
Alt rs137852741(G,T;G,T)
Reference rs137852741(C;C)
Significance Pathogenic
Disease Primary pulmonary hypertension
Variation info
Gene BMPR2
CLNDBN Primary pulmonary hypertension
Reversed 0
HGVS NC_000002.11:g.203421083C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009341.2,