rs773770609

Orientation

plus

Stabilized

plus

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

Make rs773770609(A;A)

Make rs773770609(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

6695784

Gene

SLC13A5

is a	snp
is	mentioned by
dbSNP	rs773770609
dbSNP (classic)	rs773770609
ClinGen	rs773770609
ebi	rs773770609
HLI	rs773770609
Exac	rs773770609
Gnomad	rs773770609
Varsome	rs773770609
LitVar	rs773770609
Map	rs773770609
PheGenI	rs773770609
Biobank	rs773770609
1000 genomes	rs773770609
hgdp	rs773770609
ensembl	rs773770609
geneview	rs773770609
scholar	rs773770609
google	rs773770609
pharmgkb	rs773770609
gwascentral	rs773770609
openSNP	rs773770609
23andMe	rs773770609
SNPshot	rs773770609
SNPdbe	rs773770609
MSV3d	rs773770609
GWAS Ctlg	rs773770609

Max Magnitude

0

ClinVar
Risk	rs773770609(A;A)
Alt	rs773770609(A;A)
Reference	Rs773770609(G;G)
Significance	Pathogenic
Disease	not provided Epileptic encephalopathy
Variation	info
Gene	SLC13A5
CLNDBN	not provided Epileptic encephalopathy, early infantile, 25
Reversed	0
HGVS	NC_000017.10:g.6599103G>A
CLNSRC
CLNACC	RCV000368574.1, RCV000416469.1,