rs1064794241

Orientation

minus

Stabilized

minus

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

Make rs1064794241(-;-)

Chromosome

5

Position

126582862

Gene

ALDH7A1

is a	snp
is	mentioned by
dbSNP	rs1064794241
dbSNP (classic)	rs1064794241
ClinGen	rs1064794241
ebi	rs1064794241
HLI	rs1064794241
Exac	rs1064794241
Gnomad	rs1064794241
Varsome	rs1064794241
LitVar	rs1064794241
Map	rs1064794241
PheGenI	rs1064794241
Biobank	rs1064794241
1000 genomes	rs1064794241
hgdp	rs1064794241
ensembl	rs1064794241
geneview	rs1064794241
scholar	rs1064794241
google	rs1064794241
pharmgkb	rs1064794241
gwascentral	rs1064794241
openSNP	rs1064794241
23andMe	rs1064794241
SNPshot	rs1064794241
SNPdbe	rs1064794241
MSV3d	rs1064794241
GWAS Ctlg	rs1064794241

Max Magnitude

3

ClinVar
Risk	rs1064794241(-;-)
Alt	rs1064794241(-;-)
Reference	Rs1064794241(TCTT;TCTT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ALDH7A1
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.125918554_125918557delAAGA
CLNSRC
CLNACC	RCV000486613.1,