rs1057517661

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1057517661(A;A)

Make rs1057517661(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

68685628

Gene	GAL, LOC107984343

is a	snp
is	mentioned by
dbSNP	rs1057517661
dbSNP (classic)	rs1057517661
ClinGen	rs1057517661
ebi	rs1057517661
HLI	rs1057517661
Exac	rs1057517661
Gnomad	rs1057517661
Varsome	rs1057517661
LitVar	rs1057517661
Map	rs1057517661
PheGenI	rs1057517661
Biobank	rs1057517661
1000 genomes	rs1057517661
hgdp	rs1057517661
ensembl	rs1057517661
geneview	rs1057517661
scholar	rs1057517661
google	rs1057517661
pharmgkb	rs1057517661
gwascentral	rs1057517661
openSNP	rs1057517661
23andMe	rs1057517661
SNPshot	rs1057517661
SNPdbe	rs1057517661
MSV3d	rs1057517661
GWAS Ctlg	rs1057517661

Max Magnitude

0

ClinVar
Risk	rs1057517661(A;A)
Alt	rs1057517661(A;A)
Reference	Rs1057517661(C;C)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	GAL
CLNDBN	Epilepsy, familial temporal lobe, 8
Reversed	0
HGVS	NC_000011.9:g.68453096C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000412584.1,