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rs137852755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852755(G;G)
Make rs137852755(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position202464852
GeneBMPR2
is asnp
is mentioned by
dbSNPrs137852755
ebirs137852755
HLIrs137852755
Exacrs137852755
Varsomers137852755
Maprs137852755
PheGenIrs137852755
hapmaprs137852755
1000 genomesrs137852755
hgdprs137852755
ensemblrs137852755
gopubmedrs137852755
geneviewrs137852755
scholarrs137852755
googlers137852755
pharmgkbrs137852755
gwascentralrs137852755
openSNPrs137852755
23andMers137852755
23andMe allrs137852755
SNP Nexus

SNPshotrs137852755
SNPdbers137852755
MSV3drs137852755
GWAS Ctlgrs137852755
Max Magnitude0
OMIM600799
Desc
Variant0022
Relatedalso
ClinVar
Risk rs137852755(G;G)
Alt rs137852755(G;G)
Reference rs137852755(T;T)
Significance Pathogenic
Disease Pulmonary venoocclusive disease 1
Variation info
Gene BMPR2
CLNDBN Pulmonary venoocclusive disease 1
Reversed 0
HGVS NC_000002.11:g.203329575T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009362.4,