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rs796051912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796051912(-;T)
Make rs796051912(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7220609
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs796051912
dbSNP (old)rs796051912
ClinGenrs796051912
ebirs796051912
HLIrs796051912
Exacrs796051912
Gnomadrs796051912
Varsomers796051912
Maprs796051912
PheGenIrs796051912
Biobankrs796051912
1000 genomesrs796051912
hgdprs796051912
ensemblrs796051912
gopubmedrs796051912
geneviewrs796051912
scholarrs796051912
googlers796051912
pharmgkbrs796051912
gwascentralrs796051912
openSNPrs796051912
23andMers796051912
23andMe allrs796051912
SNP Nexus

SNPshotrs796051912
SNPdbers796051912
MSV3drs796051912
GWAS Ctlgrs796051912
Max Magnitude0
ClinVar
Risk rs796051912(T;T)
Alt rs796051912(T;T)
Reference Rs796051912(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7123928dupT
CLNSRC
CLNACC RCV000185734.1,