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rs533055438

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs533055438(A;A)
Make rs533055438(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7223859
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs533055438
ebirs533055438
HLIrs533055438
Exacrs533055438
Varsomers533055438
Maprs533055438
PheGenIrs533055438
hapmaprs533055438
1000 genomesrs533055438
hgdprs533055438
ensemblrs533055438
gopubmedrs533055438
geneviewrs533055438
scholarrs533055438
googlers533055438
pharmgkbrs533055438
gwascentralrs533055438
openSNPrs533055438
23andMers533055438
23andMe allrs533055438
SNP Nexus

SNPshotrs533055438
SNPdbers533055438
MSV3drs533055438
GWAS Ctlgrs533055438
Max Magnitude0
ClinVar
Risk rs533055438(A;A)
Alt rs533055438(A;A)
Reference rs533055438(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL MIR324
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7127178G>A
CLNSRC
CLNACC RCV000185723.2,