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rs794727773

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727773(G;T)
Make rs794727773(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7221008
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs794727773
ebirs794727773
HLIrs794727773
Exacrs794727773
Varsomers794727773
Maprs794727773
PheGenIrs794727773
hapmaprs794727773
1000 genomesrs794727773
hgdprs794727773
ensemblrs794727773
gopubmedrs794727773
geneviewrs794727773
scholarrs794727773
googlers794727773
pharmgkbrs794727773
gwascentralrs794727773
openSNPrs794727773
23andMers794727773
23andMe allrs794727773
SNP Nexus

SNPshotrs794727773
SNPdbers794727773
MSV3drs794727773
GWAS Ctlgrs794727773
Max Magnitude0
ClinVar
Risk rs794727773(A,T;A,T)
Alt rs794727773(A,T;A,T)
Reference rs794727773(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7124327G>A; NC_000017.10:g.7124327G>T
CLNSRC
CLNACC RCV000185710.1, RCV000179233.1,