rs1064794774

Orientation

minus

Stabilized

minus

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

Make rs1064794774(A;A)

Chromosome

5

Position

126546338

Gene

ALDH7A1

is a	snp
is	mentioned by
dbSNP	rs1064794774
dbSNP (classic)	rs1064794774
ClinGen	rs1064794774
ebi	rs1064794774
HLI	rs1064794774
Exac	rs1064794774
Gnomad	rs1064794774
Varsome	rs1064794774
LitVar	rs1064794774
Map	rs1064794774
PheGenI	rs1064794774
Biobank	rs1064794774
1000 genomes	rs1064794774
hgdp	rs1064794774
ensembl	rs1064794774
geneview	rs1064794774
scholar	rs1064794774
google	rs1064794774
pharmgkb	rs1064794774
gwascentral	rs1064794774
openSNP	rs1064794774
23andMe	rs1064794774
SNPshot	rs1064794774
SNPdbe	rs1064794774
MSV3d	rs1064794774
GWAS Ctlg	rs1064794774

Max Magnitude

3

ClinVar
Risk	rs1064794774(A;A)
Alt	rs1064794774(A;A)
Reference	Rs1064794774(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALDH7A1
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.125882030C>T
CLNSRC
CLNACC	RCV000479462.1,