Have questions? Visit https://www.reddit.com/r/SNPedia

rs796051916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796051916(-;C)
Make rs796051916(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7224010
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs796051916
ClinGenrs796051916
ebirs796051916
HLIrs796051916
Exacrs796051916
Varsomers796051916
Maprs796051916
PheGenIrs796051916
hapmaprs796051916
1000 genomesrs796051916
hgdprs796051916
ensemblrs796051916
gopubmedrs796051916
geneviewrs796051916
scholarrs796051916
googlers796051916
pharmgkbrs796051916
gwascentralrs796051916
openSNPrs796051916
23andMers796051916
23andMe allrs796051916
SNP Nexus

SNPshotrs796051916
SNPdbers796051916
MSV3drs796051916
GWAS Ctlgrs796051916
Max Magnitude0
ClinVar
Risk rs796051916(C;C)
Alt rs796051916(C;C)
Reference Rs796051916(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADVL MIR324
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7127329dupC
CLNSRC
CLNACC RCV000185739.1,