rs386419981

Orientation

minus

Stabilized

minus

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

Make rs386419981(C;C)

Make rs386419981(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14891

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs386419981
dbSNP (classic)	rs386419981
ClinGen	rs386419981
ebi	rs386419981
HLI	rs386419981
Exac	rs386419981
Gnomad	rs386419981
Varsome	rs386419981
LitVar	rs386419981
Map	rs386419981
PheGenI	rs386419981
Biobank	rs386419981
1000 genomes	rs386419981
hgdp	rs386419981
ensembl	rs386419981
geneview	rs386419981
scholar	rs386419981
google	rs386419981
pharmgkb	rs386419981
gwascentral	rs386419981
openSNP	rs386419981
23andMe	rs386419981
SNPshot	rs386419981
SNPdbe	rs386419981
MSV3d	rs386419981
GWAS Ctlg	rs386419981

Merged from

Rs527236165

Max Magnitude

0

ClinVar
Risk	rs386419981(C;C)
Alt	rs386419981(C;C)
Reference	Rs386419981(G;G)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	CYTB
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_012920.1:m.14891C>G
CLNSRC
CLNACC	RCV000133407.1,