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rs374694591

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374694591(C;C)
Make rs374694591(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position202518997
GeneBMPR2
is asnp
is mentioned by
dbSNPrs374694591
ebirs374694591
HLIrs374694591
Exacrs374694591
Varsomers374694591
Maprs374694591
PheGenIrs374694591
hapmaprs374694591
1000 genomesrs374694591
hgdprs374694591
ensemblrs374694591
gopubmedrs374694591
geneviewrs374694591
scholarrs374694591
googlers374694591
pharmgkbrs374694591
gwascentralrs374694591
openSNPrs374694591
23andMers374694591
23andMe allrs374694591
SNP Nexus

SNPshotrs374694591
SNPdbers374694591
MSV3drs374694591
GWAS Ctlgrs374694591
Max Magnitude0
ClinVar
Risk rs374694591(C;C)
Alt rs374694591(C;C)
Reference rs374694591(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BMPR2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.203383720G>C
CLNSRC
CLNACC RCV000196055.1,