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rs796051915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796051915(-;G)
Make rs796051915(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7223859
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs796051915
dbSNP (old)rs796051915
ClinGenrs796051915
ebirs796051915
HLIrs796051915
Exacrs796051915
Gnomadrs796051915
Varsomers796051915
Maprs796051915
PheGenIrs796051915
Biobankrs796051915
1000 genomesrs796051915
hgdprs796051915
ensemblrs796051915
gopubmedrs796051915
geneviewrs796051915
scholarrs796051915
googlers796051915
pharmgkbrs796051915
gwascentralrs796051915
openSNPrs796051915
23andMers796051915
23andMe allrs796051915
SNP Nexus

SNPshotrs796051915
SNPdbers796051915
MSV3drs796051915
GWAS Ctlgrs796051915
Max Magnitude0
ClinVar
Risk rs796051915(G;G)
Alt rs796051915(G;G)
Reference Rs796051915(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL MIR324
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7127178dupG
CLNSRC
CLNACC RCV000185738.1,