rs1057516072

Orientation

plus

Stabilized

plus

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

Make rs1057516072(A;A)

Make rs1057516072(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15060

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs1057516072
dbSNP (classic)	rs1057516072
ClinGen	rs1057516072
ebi	rs1057516072
HLI	rs1057516072
Exac	rs1057516072
Gnomad	rs1057516072
Varsome	rs1057516072
LitVar	rs1057516072
Map	rs1057516072
PheGenI	rs1057516072
Biobank	rs1057516072
1000 genomes	rs1057516072
hgdp	rs1057516072
ensembl	rs1057516072
geneview	rs1057516072
scholar	rs1057516072
google	rs1057516072
pharmgkb	rs1057516072
gwascentral	rs1057516072
openSNP	rs1057516072
23andMe	rs1057516072
SNPshot	rs1057516072
SNPdbe	rs1057516072
MSV3d	rs1057516072
GWAS Ctlg	rs1057516072

Max Magnitude

0

ClinVar
Risk	rs1057516072(A;A)
Alt	rs1057516072(A;A)
Reference	Rs1057516072(G;G)
Significance	Probable-Pathogenic
Disease	Bilateral lesions of basal ganglia Seizure Disorders
Variation	info
Gene	CYTB
CLNDBN	Bilateral lesions of basal ganglia Seizure Disorders
Reversed	0
HGVS	NC_012920.1:m.15060G>A
CLNSRC
CLNACC	RCV000408920.1,