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rs112406105

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs112406105(C;C)
Make rs112406105(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7223152
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs112406105
ebirs112406105
HLIrs112406105
Exacrs112406105
Varsomers112406105
Maprs112406105
PheGenIrs112406105
hapmaprs112406105
1000 genomesrs112406105
hgdprs112406105
ensemblrs112406105
gopubmedrs112406105
geneviewrs112406105
scholarrs112406105
googlers112406105
pharmgkbrs112406105
gwascentralrs112406105
openSNPrs112406105
23andMers112406105
23andMe allrs112406105
SNP Nexus

SNPshotrs112406105
SNPdbers112406105
MSV3drs112406105
GWAS Ctlgrs112406105
Max Magnitude0
ClinVar
Risk rs112406105(A,C;A,C)
Alt rs112406105(A,C;A,C)
Reference rs112406105(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR324 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7126471G>A
CLNSRC
CLNACC RCV000185720.2,