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rs1085307432

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome9
Position127818810
GeneENG, LOC102723566
is asnp
is mentioned by
dbSNPrs1085307432
dbSNP (old)rs1085307432
ClinGenrs1085307432
ebirs1085307432
HLIrs1085307432
Exacrs1085307432
Gnomadrs1085307432
Varsomers1085307432
Maprs1085307432
PheGenIrs1085307432
Biobankrs1085307432
1000 genomesrs1085307432
hgdprs1085307432
ensemblrs1085307432
gopubmedrs1085307432
geneviewrs1085307432
scholarrs1085307432
googlers1085307432
pharmgkbrs1085307432
gwascentralrs1085307432
openSNPrs1085307432
23andMers1085307432
23andMe allrs1085307432
SNPshotrs1085307432
SNPdbers1085307432
MSV3drs1085307432
GWAS Ctlgrs1085307432
Max Magnitude0
ClinVar
Risk rs1085307432(-;-)
Alt rs1085307432(-;-)
Reference Rs1085307432(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.130581089delA
CLNSRC
CLNACC RCV000488464.1,