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rs1085307435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome9
Position127815991
GeneENG, LOC102723566
is asnp
is mentioned by
dbSNPrs1085307435
dbSNP (old)rs1085307435
ClinGenrs1085307435
ebirs1085307435
HLIrs1085307435
Exacrs1085307435
Gnomadrs1085307435
Varsomers1085307435
Maprs1085307435
PheGenIrs1085307435
Biobankrs1085307435
1000 genomesrs1085307435
hgdprs1085307435
ensemblrs1085307435
gopubmedrs1085307435
geneviewrs1085307435
scholarrs1085307435
googlers1085307435
pharmgkbrs1085307435
gwascentralrs1085307435
openSNPrs1085307435
23andMers1085307435
23andMe allrs1085307435
SNPshotrs1085307435
SNPdbers1085307435
MSV3drs1085307435
GWAS Ctlgrs1085307435
Max Magnitude0
ClinVar
Risk rs1085307435(-;-)
Alt rs1085307435(-;-)
Reference Rs1085307435(A;A)
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.130578270delT
CLNSRC
CLNACC RCV000488618.1,