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rs117356004

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs117356004(A;A)
Make rs117356004(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position120737097
GeneACADS
is asnp
is mentioned by
dbSNPrs117356004
dbSNP (old)rs117356004
ClinGenrs117356004
ebirs117356004
HLIrs117356004
Exacrs117356004
Gnomadrs117356004
Varsomers117356004
Maprs117356004
PheGenIrs117356004
Biobankrs117356004
1000 genomesrs117356004
hgdprs117356004
ensemblrs117356004
gopubmedrs117356004
geneviewrs117356004
scholarrs117356004
googlers117356004
pharmgkbrs117356004
gwascentralrs117356004
openSNPrs117356004
23andMers117356004
23andMe allrs117356004
SNPshotrs117356004
SNPdbers117356004
MSV3drs117356004
GWAS Ctlgrs117356004
Max Magnitude0
ClinVar
Risk rs117356004(A;A)
Alt rs117356004(A;A)
Reference Rs117356004(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121174900G>A
CLNSRC
CLNACC RCV000442937.1,