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rs1001298373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position120737077
GeneACADS
is asnp
is mentioned by
dbSNPrs1001298373
dbSNP (old)rs1001298373
ClinGenrs1001298373
ebirs1001298373
HLIrs1001298373
Exacrs1001298373
Gnomadrs1001298373
Varsomers1001298373
Maprs1001298373
PheGenIrs1001298373
Biobankrs1001298373
1000 genomesrs1001298373
hgdprs1001298373
ensemblrs1001298373
gopubmedrs1001298373
geneviewrs1001298373
scholarrs1001298373
googlers1001298373
pharmgkbrs1001298373
gwascentralrs1001298373
openSNPrs1001298373
23andMers1001298373
23andMe allrs1001298373
SNP Nexus

SNPshotrs1001298373
SNPdbers1001298373
MSV3drs1001298373
GWAS Ctlgrs1001298373
Max Magnitude0
ClinVar
Risk rs1001298373(T;T)
Alt rs1001298373(T;T)
Reference Rs1001298373(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121174880C>T
CLNSRC
CLNACC RCV000489562.1,