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rs188985665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs188985665(A;A)
Make rs188985665(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178014388
GenePDE11A
is asnp
is mentioned by
dbSNPrs188985665
dbSNP (old)rs188985665
ClinGenrs188985665
ebirs188985665
HLIrs188985665
Exacrs188985665
Gnomadrs188985665
Varsomers188985665
Maprs188985665
PheGenIrs188985665
Biobankrs188985665
1000 genomesrs188985665
hgdprs188985665
ensemblrs188985665
gopubmedrs188985665
geneviewrs188985665
scholarrs188985665
googlers188985665
pharmgkbrs188985665
gwascentralrs188985665
openSNPrs188985665
23andMers188985665
23andMe allrs188985665
SNPshotrs188985665
SNPdbers188985665
MSV3drs188985665
GWAS Ctlgrs188985665
Max Magnitude0
ClinVar
Risk rs188985665(A;A)
Alt rs188985665(A;A)
Reference Rs188985665(G;G)
Significance Probable-Pathogenic
Disease Pigmented nodular adrenocortical disease
Variation info
Gene PDE11A
CLNDBN Pigmented nodular adrenocortical disease, primary, 2
Reversed 0
HGVS NC_000002.11:g.178879115G>A
CLNSRC
CLNACC RCV000490398.1,