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rs200573371

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200573371(A;A)
Make rs200573371(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7222669
GeneACADVL
is asnp
is mentioned by
dbSNPrs200573371
ebirs200573371
HLIrs200573371
Exacrs200573371
Varsomers200573371
Maprs200573371
PheGenIrs200573371
hapmaprs200573371
1000 genomesrs200573371
hgdprs200573371
ensemblrs200573371
gopubmedrs200573371
geneviewrs200573371
scholarrs200573371
googlers200573371
pharmgkbrs200573371
gwascentralrs200573371
openSNPrs200573371
23andMers200573371
23andMe allrs200573371
SNP Nexus

SNPshotrs200573371
SNPdbers200573371
MSV3drs200573371
GWAS Ctlgrs200573371
Max Magnitude0
ClinVar
Risk rs200573371(A;A)
Alt rs200573371(A;A)
Reference rs200573371(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7125988G>A
CLNSRC
CLNACC RCV000185715.1,