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rs1064794053

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;G) 3 Carrier of a pyridoxine-dependent epilepsy mutation
(G;G) 0 common in clinvar


Make rs1064794053(C;C)
Chromosome5
Position126582975
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs1064794053
dbSNP (classic)rs1064794053
ClinGenrs1064794053
ebirs1064794053
HLIrs1064794053
Exacrs1064794053
Gnomadrs1064794053
Varsomers1064794053
LitVarrs1064794053
Maprs1064794053
PheGenIrs1064794053
Biobankrs1064794053
1000 genomesrs1064794053
hgdprs1064794053
ensemblrs1064794053
geneviewrs1064794053
scholarrs1064794053
googlers1064794053
pharmgkbrs1064794053
gwascentralrs1064794053
openSNPrs1064794053
23andMers1064794053
SNPshotrs1064794053
SNPdbers1064794053
MSV3drs1064794053
GWAS Ctlgrs1064794053
Max Magnitude3
ClinVar
Risk rs1064794053(C;C)
Alt rs1064794053(C;C)
Reference Rs1064794053(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH7A1
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.125918667C>G
CLNSRC
CLNACC RCV000481389.1,