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rs1085307434

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome9
Position127816075
GeneENG, LOC102723566
is asnp
is mentioned by
dbSNPrs1085307434
dbSNP (old)rs1085307434
ClinGenrs1085307434
ebirs1085307434
HLIrs1085307434
Exacrs1085307434
Gnomadrs1085307434
Varsomers1085307434
Maprs1085307434
PheGenIrs1085307434
Biobankrs1085307434
1000 genomesrs1085307434
hgdprs1085307434
ensemblrs1085307434
gopubmedrs1085307434
geneviewrs1085307434
scholarrs1085307434
googlers1085307434
pharmgkbrs1085307434
gwascentralrs1085307434
openSNPrs1085307434
23andMers1085307434
23andMe allrs1085307434
SNPshotrs1085307434
SNPdbers1085307434
MSV3drs1085307434
GWAS Ctlgrs1085307434
Max Magnitude0
ClinVar
Risk rs1085307434(C;C)
Alt rs1085307434(C;C)
Reference Rs1085307434(T;T)
Significance Pathogenic
Disease Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia
Variation info
Gene ENG LOC102723566
CLNDBN Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia
Reversed 1
HGVS NC_000009.11:g.130578354A>G
CLNSRC
CLNACC RCV000488489.1,