Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs200620279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200620279(A;A)
Make rs200620279(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position134261756
GeneACAD8
is asnp
is mentioned by
dbSNPrs200620279
dbSNP (old)rs200620279
ClinGenrs200620279
ebirs200620279
HLIrs200620279
Exacrs200620279
Gnomadrs200620279
Varsomers200620279
Maprs200620279
PheGenIrs200620279
Biobankrs200620279
1000 genomesrs200620279
hgdprs200620279
ensemblrs200620279
gopubmedrs200620279
geneviewrs200620279
scholarrs200620279
googlers200620279
pharmgkbrs200620279
gwascentralrs200620279
openSNPrs200620279
23andMers200620279
23andMe allrs200620279
SNPshotrs200620279
SNPdbers200620279
MSV3drs200620279
GWAS Ctlgrs200620279
Max Magnitude0
ClinVar
Risk rs200620279(A;A)
Alt rs200620279(A;A)
Reference Rs200620279(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACAD8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.134131650G>A
CLNSRC
CLNACC RCV000414228.1,