rs527236164

Orientation

plus

Stabilized

plus

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

Make rs527236164(C;T)

Make rs527236164(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14800

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs527236164
dbSNP (classic)	rs527236164
ClinGen	rs527236164
ebi	rs527236164
HLI	rs527236164
Exac	rs527236164
Gnomad	rs527236164
Varsome	rs527236164
LitVar	rs527236164
Map	rs527236164
PheGenI	rs527236164
Biobank	rs527236164
1000 genomes	rs527236164
hgdp	rs527236164
ensembl	rs527236164
geneview	rs527236164
scholar	rs527236164
google	rs527236164
pharmgkb	rs527236164
gwascentral	rs527236164
openSNP	rs527236164
23andMe	rs527236164
SNPshot	rs527236164
SNPdbe	rs527236164
MSV3d	rs527236164
GWAS Ctlg	rs527236164

Max Magnitude

0

ClinVar
Risk	rs527236164(T;T)
Alt	rs527236164(T;T)
Reference	Rs527236164(C;C)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	CYTB
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_012920.1:m.14800C>T
CLNSRC	ClinVar
CLNACC	RCV000133406.1,