rs797045969

Orientation

minus

Stabilized

minus

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

Make rs797045969(C;T)

Make rs797045969(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

792722

Gene

SLC25A22

is a	snp
is	mentioned by
dbSNP	rs797045969
dbSNP (classic)	rs797045969
ClinGen	rs797045969
ebi	rs797045969
HLI	rs797045969
Exac	rs797045969
Gnomad	rs797045969
Varsome	rs797045969
LitVar	rs797045969
Map	rs797045969
PheGenI	rs797045969
Biobank	rs797045969
1000 genomes	rs797045969
hgdp	rs797045969
ensembl	rs797045969
geneview	rs797045969
scholar	rs797045969
google	rs797045969
pharmgkb	rs797045969
gwascentral	rs797045969
openSNP	rs797045969
23andMe	rs797045969
SNPshot	rs797045969
SNPdbe	rs797045969
MSV3d	rs797045969
GWAS Ctlg	rs797045969

Max Magnitude

0

ClinVar
Risk	rs797045969(T;T)
Alt	rs797045969(T;T)
Reference	Rs797045969(C;C)
Significance	Pathogenic
Disease	Early myoclonic encephalopathy
Variation	info
Gene	SLC25A22
CLNDBN	Early myoclonic encephalopathy
Reversed	1
HGVS	NC_000011.9:g.792722G>A
CLNSRC
CLNACC	RCV000194231.1,