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rs398123081

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123081(C;C)
Make rs398123081(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7223980
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs398123081
ebirs398123081
HLIrs398123081
Exacrs398123081
Varsomers398123081
Maprs398123081
PheGenIrs398123081
hapmaprs398123081
1000 genomesrs398123081
hgdprs398123081
ensemblrs398123081
gopubmedrs398123081
geneviewrs398123081
scholarrs398123081
googlers398123081
pharmgkbrs398123081
gwascentralrs398123081
openSNPrs398123081
23andMers398123081
23andMe allrs398123081
SNP Nexus

SNPshotrs398123081
SNPdbers398123081
MSV3drs398123081
GWAS Ctlgrs398123081
Max Magnitude0
ClinVar
Risk rs398123081(C;C)
Alt rs398123081(C;C)
Reference rs398123081(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR324 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7127299G>A; NC_000017.10:g.7127299G>C
CLNSRC
CLNACC RCV000185724.1, RCV000077904.4,