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rs1064796104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Chromosome17
Position7221662
GeneACADVL, DLG4
is asnp
is mentioned by
dbSNPrs1064796104
dbSNP (classic)rs1064796104
ClinGenrs1064796104
ebirs1064796104
HLIrs1064796104
Exacrs1064796104
Gnomadrs1064796104
Varsomers1064796104
LitVarrs1064796104
Maprs1064796104
PheGenIrs1064796104
Biobankrs1064796104
1000 genomesrs1064796104
hgdprs1064796104
ensemblrs1064796104
geneviewrs1064796104
scholarrs1064796104
googlers1064796104
pharmgkbrs1064796104
gwascentralrs1064796104
openSNPrs1064796104
23andMers1064796104
SNPshotrs1064796104
SNPdbers1064796104
MSV3drs1064796104
GWAS Ctlgrs1064796104
Max Magnitude0
ClinVar
Risk rs1064796104(-;-)
Alt rs1064796104(-;-)
Reference Rs1064796104(AC;AC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLG4 ACADVL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7124981_7124982delAC
CLNSRC
CLNACC RCV000487087.1,