rs207459997

Orientation

plus

Stabilized

plus

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

Make rs207459997(A;A)

Make rs207459997(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15615

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs207459997
dbSNP (classic)	rs207459997
ClinGen	rs207459997
ebi	rs207459997
HLI	rs207459997
Exac	rs207459997
Gnomad	rs207459997
Varsome	rs207459997
LitVar	rs207459997
Map	rs207459997
PheGenI	rs207459997
Biobank	rs207459997
1000 genomes	rs207459997
hgdp	rs207459997
ensembl	rs207459997
geneview	rs207459997
scholar	rs207459997
google	rs207459997
pharmgkb	rs207459997
gwascentral	rs207459997
openSNP	rs207459997
23andMe	rs207459997
SNPshot	rs207459997
SNPdbe	rs207459997
MSV3d	rs207459997
GWAS Ctlg	rs207459997

Max Magnitude

0

ClinVar
Risk	rs207459997(A;A)
Alt	rs207459997(A;A)
Reference	Rs207459997(G;G)
Significance	Pathogenic
Disease	Exercise intolerance
Variation	info
Gene	CYTB
CLNDBN	Exercise intolerance
Reversed	0
HGVS	NC_012920.1:m.15615G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010316.4,