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rs796051917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs796051917(-;-)
Make rs796051917(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7224863
GeneACADVL, DVL2, MIR324
is asnp
is mentioned by
dbSNPrs796051917
ClinGenrs796051917
ebirs796051917
HLIrs796051917
Exacrs796051917
Varsomers796051917
Maprs796051917
PheGenIrs796051917
hapmaprs796051917
1000 genomesrs796051917
hgdprs796051917
ensemblrs796051917
gopubmedrs796051917
geneviewrs796051917
scholarrs796051917
googlers796051917
pharmgkbrs796051917
gwascentralrs796051917
openSNPrs796051917
23andMers796051917
23andMe allrs796051917
SNP Nexus

SNPshotrs796051917
SNPdbers796051917
MSV3drs796051917
GWAS Ctlgrs796051917
Max Magnitude0
ClinVar
Risk rs796051917(-;-)
Alt rs796051917(-;-)
Reference Rs796051917(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR324 ACADVL DVL2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7128182_7128183delCT
CLNSRC
CLNACC RCV000185740.1,