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rs758753966

From SNPedia

Orientationplus
Stabilizedplus
Make rs758753966(A;C)
Make rs758753966(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position75761120
GeneACADM
is asnp
is mentioned by
dbSNPrs758753966
dbSNP (classic)rs758753966
ClinGenrs758753966
ebirs758753966
HLIrs758753966
Exacrs758753966
Gnomadrs758753966
Varsomers758753966
LitVarrs758753966
Maprs758753966
PheGenIrs758753966
Biobankrs758753966
1000 genomesrs758753966
hgdprs758753966
ensemblrs758753966
geneviewrs758753966
scholarrs758753966
googlers758753966
pharmgkbrs758753966
gwascentralrs758753966
openSNPrs758753966
23andMers758753966
SNPshotrs758753966
SNPdbers758753966
MSV3drs758753966
GWAS Ctlgrs758753966
Max Magnitude0
ClinVar
Risk rs758753966(C;C)
Alt rs758753966(C;C)
Reference Rs758753966(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76226805A>C
CLNSRC
CLNACC RCV000255491.1,