rs527236201

Orientation

plus

Stabilized

plus

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

Make rs527236201(A;A)

Make rs527236201(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15349

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs527236201
dbSNP (classic)	rs527236201
ClinGen	rs527236201
ebi	rs527236201
HLI	rs527236201
Exac	rs527236201
Gnomad	rs527236201
Varsome	rs527236201
LitVar	rs527236201
Map	rs527236201
PheGenI	rs527236201
Biobank	rs527236201
1000 genomes	rs527236201
hgdp	rs527236201
ensembl	rs527236201
geneview	rs527236201
scholar	rs527236201
google	rs527236201
pharmgkb	rs527236201
gwascentral	rs527236201
openSNP	rs527236201
23andMe	rs527236201
SNPshot	rs527236201
SNPdbe	rs527236201
MSV3d	rs527236201
GWAS Ctlg	rs527236201

Max Magnitude

0

ClinVar
Risk	rs527236201(A;A) rs527236201(T;T)
Alt	rs527236201(A;A) rs527236201(T;T)
Reference	Rs527236201(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.15349C>A; NC_012920.1:m.15349C>T
CLNSRC	ClinVar
CLNACC	RCV000133423.1, RCV000133424.1,