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rs121912707

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912707(C;C)
Make rs121912707(C;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position126552059
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs121912707
ebirs121912707
HLIrs121912707
Exacrs121912707
Varsomers121912707
Maprs121912707
PheGenIrs121912707
hapmaprs121912707
1000 genomesrs121912707
hgdprs121912707
ensemblrs121912707
gopubmedrs121912707
geneviewrs121912707
scholarrs121912707
googlers121912707
pharmgkbrs121912707
gwascentralrs121912707
openSNPrs121912707
23andMers121912707
23andMe allrs121912707
SNP Nexus

SNPshotrs121912707
SNPdbers121912707
MSV3drs121912707
GWAS Ctlgrs121912707
GMAF0.0004591
Max Magnitude0
OMIM107323
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912707(C;C)
Alt rs121912707(C;C)
Reference rs121912707(G;G)
Significance Other
Disease Pyridoxine-dependent epilepsy not provided
Variation info
Gene ALDH7A1
CLNDBN Pyridoxine-dependent epilepsy not provided
Reversed 1
HGVS NC_000005.9:g.125887751C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019610.29, RCV000186744.2,