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rs150321966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150321966(A;A)
Make rs150321966(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position133366990
GeneECHS1
is asnp
is mentioned by
dbSNPrs150321966
dbSNP (old)rs150321966
ClinGenrs150321966
ebirs150321966
HLIrs150321966
Exacrs150321966
Gnomadrs150321966
Varsomers150321966
LitVarrs150321966
Maprs150321966
PheGenIrs150321966
Biobankrs150321966
1000 genomesrs150321966
hgdprs150321966
ensemblrs150321966
gopubmedrs150321966
geneviewrs150321966
scholarrs150321966
googlers150321966
pharmgkbrs150321966
gwascentralrs150321966
openSNPrs150321966
23andMers150321966
23andMe allrs150321966
SNPshotrs150321966
SNPdbers150321966
MSV3drs150321966
GWAS Ctlgrs150321966
Max Magnitude0
ClinVar
Risk rs150321966(A;A)
Alt rs150321966(A;A)
Reference Rs150321966(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ECHS1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.135180494G>A
CLNSRC
CLNACC RCV000421257.1,