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rs796051908

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051908(C;T)
Make rs796051908(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7221542
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs796051908
ebirs796051908
HLIrs796051908
Exacrs796051908
Varsomers796051908
Maprs796051908
PheGenIrs796051908
hapmaprs796051908
1000 genomesrs796051908
hgdprs796051908
ensemblrs796051908
gopubmedrs796051908
geneviewrs796051908
scholarrs796051908
googlers796051908
pharmgkbrs796051908
gwascentralrs796051908
openSNPrs796051908
23andMers796051908
23andMe allrs796051908
SNP Nexus

SNPshotrs796051908
SNPdbers796051908
MSV3drs796051908
GWAS Ctlgrs796051908
Max Magnitude0
ClinVar
Risk rs796051908(T;T)
Alt rs796051908(T;T)
Reference rs796051908(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7124861C>T
CLNSRC
CLNACC RCV000185711.2,