rs587777577

Orientation

plus

Stabilized

plus

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

Make rs587777577(A;A)

Make rs587777577(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

6703006

Gene

SLC13A5

is a	snp
is	mentioned by
dbSNP	rs587777577
dbSNP (classic)	rs587777577
ClinGen	rs587777577
ebi	rs587777577
HLI	rs587777577
Exac	rs587777577
Gnomad	rs587777577
Varsome	rs587777577
LitVar	rs587777577
Map	rs587777577
PheGenI	rs587777577
Biobank	rs587777577
1000 genomes	rs587777577
hgdp	rs587777577
ensembl	rs587777577
geneview	rs587777577
scholar	rs587777577
google	rs587777577
pharmgkb	rs587777577
gwascentral	rs587777577
openSNP	rs587777577
23andMe	rs587777577
SNPshot	rs587777577
SNPdbe	rs587777577
MSV3d	rs587777577
GWAS Ctlg	rs587777577

Max Magnitude

0

ClinVar
Risk	rs587777577(A;A)
Alt	rs587777577(A;A)
Reference	Rs587777577(G;G)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	SLC13A5
CLNDBN	Epileptic encephalopathy, early infantile, 25
Reversed	0
HGVS	NC_000017.10:g.6606325G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128861.5,