rs527236168

Orientation

plus

Stabilized

plus

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

Make rs527236168(C;T)

Make rs527236168(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14974

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs527236168
dbSNP (classic)	rs527236168
ClinGen	rs527236168
ebi	rs527236168
HLI	rs527236168
Exac	rs527236168
Gnomad	rs527236168
Varsome	rs527236168
LitVar	rs527236168
Map	rs527236168
PheGenI	rs527236168
Biobank	rs527236168
1000 genomes	rs527236168
hgdp	rs527236168
ensembl	rs527236168
geneview	rs527236168
scholar	rs527236168
google	rs527236168
pharmgkb	rs527236168
gwascentral	rs527236168
openSNP	rs527236168
23andMe	rs527236168
SNPshot	rs527236168
SNPdbe	rs527236168
MSV3d	rs527236168
GWAS Ctlg	rs527236168

Max Magnitude

0

ClinVar
Risk	rs527236168(G;G) rs527236168(T;T)
Alt	rs527236168(G;G) rs527236168(T;T)
Reference	Rs527236168(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.14974C>G
CLNSRC	ClinVar
CLNACC	RCV000133410.1,