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rs796051914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs796051914(-;-)
Make rs796051914(-;GAG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7222677
GeneACADVL
is asnp
is mentioned by
dbSNPrs796051914
dbSNP (old)rs796051914
ClinGenrs796051914
ebirs796051914
HLIrs796051914
Exacrs796051914
Gnomadrs796051914
Varsomers796051914
Maprs796051914
PheGenIrs796051914
Biobankrs796051914
1000 genomesrs796051914
hgdprs796051914
ensemblrs796051914
gopubmedrs796051914
geneviewrs796051914
scholarrs796051914
googlers796051914
pharmgkbrs796051914
gwascentralrs796051914
openSNPrs796051914
23andMers796051914
23andMe allrs796051914
SNP Nexus

SNPshotrs796051914
SNPdbers796051914
MSV3drs796051914
GWAS Ctlgrs796051914
Max Magnitude0
ClinVar
Risk rs796051914(-;-)
Alt rs796051914(-;-)
Reference Rs796051914(GAG;GAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7125996_7125998delGAG
CLNSRC
CLNACC RCV000185737.2,