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rs796051913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGG;AGG) 0 common in clinvar
(GAG;GAG) 0 common in clinvar
Make rs796051913(-;-)
Make rs796051913(-;GAG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7222253
GeneACADVL
is asnp
is mentioned by
dbSNPrs796051913
dbSNP (old)rs796051913
ClinGenrs796051913
ebirs796051913
HLIrs796051913
Exacrs796051913
Varsomers796051913
Maprs796051913
PheGenIrs796051913
Biobankrs796051913
1000 genomesrs796051913
hgdprs796051913
ensemblrs796051913
gopubmedrs796051913
geneviewrs796051913
scholarrs796051913
googlers796051913
pharmgkbrs796051913
gwascentralrs796051913
openSNPrs796051913
23andMers796051913
23andMe allrs796051913
SNP Nexus

SNPshotrs796051913
SNPdbers796051913
MSV3drs796051913
GWAS Ctlgrs796051913
Max Magnitude0
ClinVar
Risk rs796051913(-;-) Rs796051913(AGG;AGG)
Alt rs796051913(-;-) Rs796051913(AGG;AGG)
Reference Rs796051913(GAG;GAG)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7125572_7125574delGAG
CLNSRC
CLNACC RCV000185735.3,