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rs151006739

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151006739(C;T)
Make rs151006739(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position133366051
GeneECHS1
is asnp
is mentioned by
dbSNPrs151006739
dbSNP (old)rs151006739
ClinGenrs151006739
ebirs151006739
HLIrs151006739
Exacrs151006739
Gnomadrs151006739
Varsomers151006739
Maprs151006739
PheGenIrs151006739
Biobankrs151006739
1000 genomesrs151006739
hgdprs151006739
ensemblrs151006739
gopubmedrs151006739
geneviewrs151006739
scholarrs151006739
googlers151006739
pharmgkbrs151006739
gwascentralrs151006739
openSNPrs151006739
23andMers151006739
23andMe allrs151006739
SNPshotrs151006739
SNPdbers151006739
MSV3drs151006739
GWAS Ctlgrs151006739
Max Magnitude0
ClinVar
Risk rs151006739(T;T)
Alt rs151006739(T;T)
Reference Rs151006739(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ECHS1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.135179555C>T
CLNSRC
CLNACC RCV000489942.1,