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rs796051918

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051918(A;A)
Make rs796051918(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7220923
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs796051918
ebirs796051918
HLIrs796051918
Exacrs796051918
Varsomers796051918
Maprs796051918
PheGenIrs796051918
hapmaprs796051918
1000 genomesrs796051918
hgdprs796051918
ensemblrs796051918
gopubmedrs796051918
geneviewrs796051918
scholarrs796051918
googlers796051918
pharmgkbrs796051918
gwascentralrs796051918
openSNPrs796051918
23andMers796051918
23andMe allrs796051918
SNP Nexus

SNPshotrs796051918
SNPdbers796051918
MSV3drs796051918
GWAS Ctlgrs796051918
Max Magnitude0
ClinVar
Risk rs796051918(A;A)
Alt rs796051918(A;A)
Reference rs796051918(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7124242G>A
CLNSRC
CLNACC RCV000185741.1,