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rs796051909

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051909(G;T)
Make rs796051909(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7221595
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs796051909
ebirs796051909
HLIrs796051909
Exacrs796051909
Varsomers796051909
Maprs796051909
PheGenIrs796051909
hapmaprs796051909
1000 genomesrs796051909
hgdprs796051909
ensemblrs796051909
gopubmedrs796051909
geneviewrs796051909
scholarrs796051909
googlers796051909
pharmgkbrs796051909
gwascentralrs796051909
openSNPrs796051909
23andMers796051909
23andMe allrs796051909
SNP Nexus

SNPshotrs796051909
SNPdbers796051909
MSV3drs796051909
GWAS Ctlgrs796051909
Max Magnitude0
ClinVar
Risk rs796051909(T;T)
Alt rs796051909(T;T)
Reference rs796051909(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7124914G>T
CLNSRC
CLNACC RCV000185712.1,