rs207460001

Orientation

plus

Stabilized

plus

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

Make rs207460001(C;C)

Make rs207460001(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15197

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs207460001
dbSNP (classic)	rs207460001
ClinGen	rs207460001
ebi	rs207460001
HLI	rs207460001
Exac	rs207460001
Gnomad	rs207460001
Varsome	rs207460001
LitVar	rs207460001
Map	rs207460001
PheGenI	rs207460001
Biobank	rs207460001
1000 genomes	rs207460001
hgdp	rs207460001
ensembl	rs207460001
geneview	rs207460001
scholar	rs207460001
google	rs207460001
pharmgkb	rs207460001
gwascentral	rs207460001
openSNP	rs207460001
23andMe	rs207460001
SNPshot	rs207460001
SNPdbe	rs207460001
MSV3d	rs207460001
GWAS Ctlg	rs207460001

Max Magnitude

0

ClinVar
Risk	rs207460001(C;C)
Alt	rs207460001(C;C)
Reference	Rs207460001(T;T)
Significance	Pathogenic
Disease	Exercise intolerance
Variation	info
Gene	CYTB
CLNDBN	Exercise intolerance
Reversed	0
HGVS	NC_012920.1:m.15197T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010320.4,