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rs35400405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs35400405(A;A)
Make rs35400405(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position127854342
GeneENG
is asnp
is mentioned by
dbSNPrs35400405
ebirs35400405
HLIrs35400405
Exacrs35400405
Varsomers35400405
Maprs35400405
PheGenIrs35400405
hapmaprs35400405
1000 genomesrs35400405
hgdprs35400405
ensemblrs35400405
gopubmedrs35400405
geneviewrs35400405
scholarrs35400405
googlers35400405
pharmgkbrs35400405
gwascentralrs35400405
openSNPrs35400405
23andMers35400405
23andMe allrs35400405
SNP Nexus

SNPshotrs35400405
SNPdbers35400405
MSV3drs35400405
GWAS Ctlgrs35400405
GMAF0.04178
Max Magnitude0

[PMID 22896741] TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients


ClinVar
Risk rs35400405(A;A)
Alt rs35400405(A;A)
Reference rs35400405(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ENG
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.130616621G>A
CLNSRC
CLNACC RCV000155541.3,