rs41504845

Orientation

plus

Stabilized

plus

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

Make rs41504845(C;T)

Make rs41504845(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15833

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs41504845
dbSNP (classic)	rs41504845
ClinGen	rs41504845
ebi	rs41504845
HLI	rs41504845
Exac	rs41504845
Gnomad	rs41504845
Varsome	rs41504845
LitVar	rs41504845
Map	rs41504845
PheGenI	rs41504845
Biobank	rs41504845
1000 genomes	rs41504845
hgdp	rs41504845
ensembl	rs41504845
geneview	rs41504845
scholar	rs41504845
google	rs41504845
pharmgkb	rs41504845
gwascentral	rs41504845
openSNP	rs41504845
23andMe	rs41504845
SNPshot	rs41504845
SNPdbe	rs41504845
MSV3d	rs41504845
GWAS Ctlg	rs41504845

GMAF

0.003742

Max Magnitude

0

haplogroups

ClinVar
Risk	rs41504845(A;A) rs41504845(G;G) rs41504845(T;T)
Alt	rs41504845(A;A) rs41504845(G;G) rs41504845(T;T)
Reference	Rs41504845(C;C)
Significance	Probable-non-pathogenic
Disease	not provided
Variation	info
Gene	CYTB
CLNDBN	not provided
Reversed	0
HGVS	NC_012920.1:m.15833C>T
CLNSRC
CLNACC	RCV000224196.1,