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rs372660425

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs372660425(C;C)
Make rs372660425(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position126577145
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs372660425
ebirs372660425
HLIrs372660425
Exacrs372660425
Varsomers372660425
Maprs372660425
PheGenIrs372660425
hapmaprs372660425
1000 genomesrs372660425
hgdprs372660425
ensemblrs372660425
gopubmedrs372660425
geneviewrs372660425
scholarrs372660425
googlers372660425
pharmgkbrs372660425
gwascentralrs372660425
openSNPrs372660425
23andMers372660425
23andMe allrs372660425
SNP Nexus

SNPshotrs372660425
SNPdbers372660425
MSV3drs372660425
GWAS Ctlgrs372660425
Max Magnitude0
ClinVar
Risk rs372660425(C;C)
Alt rs372660425(C;C)
Reference rs372660425(T;T)
Significance Pathogenic
Disease Pyridoxine-dependent epilepsy
Variation info
Gene ALDH7A1
CLNDBN Pyridoxine-dependent epilepsy
Reversed 0
HGVS NC_000005.9:g.125912837T>C
CLNSRC
CLNACC RCV000206803.1,