rs207460000

Orientation

plus

Stabilized

plus

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

Make rs207460000(A;A)

Make rs207460000(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15150

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs207460000
dbSNP (classic)	rs207460000
ClinGen	rs207460000
ebi	rs207460000
HLI	rs207460000
Exac	rs207460000
Gnomad	rs207460000
Varsome	rs207460000
LitVar	rs207460000
Map	rs207460000
PheGenI	rs207460000
Biobank	rs207460000
1000 genomes	rs207460000
hgdp	rs207460000
ensembl	rs207460000
geneview	rs207460000
scholar	rs207460000
google	rs207460000
pharmgkb	rs207460000
gwascentral	rs207460000
openSNP	rs207460000
23andMe	rs207460000
SNPshot	rs207460000
SNPdbe	rs207460000
MSV3d	rs207460000
GWAS Ctlg	rs207460000

Max Magnitude

0

ClinVar
Risk	rs207460000(A;A)
Alt	rs207460000(A;A)
Reference	Rs207460000(G;G)
Significance	Pathogenic
Disease	Exercise intolerance
Variation	info
Gene	CYTB
CLNDBN	Exercise intolerance
Reversed	0
HGVS	NC_012920.1:m.15150G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010319.4,