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rs138686233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138686233(C;T)
Make rs138686233(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position176945951
GeneASTN1
is asnp
is mentioned by
dbSNPrs138686233
dbSNP (old)rs138686233
ClinGenrs138686233
ebirs138686233
HLIrs138686233
Exacrs138686233
Gnomadrs138686233
Varsomers138686233
Maprs138686233
PheGenIrs138686233
Biobankrs138686233
1000 genomesrs138686233
hgdprs138686233
ensemblrs138686233
gopubmedrs138686233
geneviewrs138686233
scholarrs138686233
googlers138686233
pharmgkbrs138686233
gwascentralrs138686233
openSNPrs138686233
23andMers138686233
23andMe allrs138686233
SNPshotrs138686233
SNPdbers138686233
MSV3drs138686233
GWAS Ctlgrs138686233
Max Magnitude0
ClinVar
Risk rs138686233(G;G) rs138686233(T;T)
Alt rs138686233(G;G) rs138686233(T;T)
Reference Rs138686233(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ASTN1
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000001.10:g.176915087C>G
CLNSRC
CLNACC RCV000454328.1,