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rs796051911

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051911(A;A)
Make rs796051911(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7222840
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs796051911
ebirs796051911
HLIrs796051911
Exacrs796051911
Varsomers796051911
Maprs796051911
PheGenIrs796051911
hapmaprs796051911
1000 genomesrs796051911
hgdprs796051911
ensemblrs796051911
gopubmedrs796051911
geneviewrs796051911
scholarrs796051911
googlers796051911
pharmgkbrs796051911
gwascentralrs796051911
openSNPrs796051911
23andMers796051911
23andMe allrs796051911
SNP Nexus

SNPshotrs796051911
SNPdbers796051911
MSV3drs796051911
GWAS Ctlgrs796051911
Max Magnitude0
ClinVar
Risk rs796051911(A;A)
Alt rs796051911(A;A)
Reference rs796051911(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR324 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7126159C>A
CLNSRC
CLNACC RCV000185718.1,