rs527236191

Orientation

plus

Stabilized

plus

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

Make rs527236191(A;G)

Make rs527236191(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15649

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs527236191
dbSNP (classic)	rs527236191
ClinGen	rs527236191
ebi	rs527236191
HLI	rs527236191
Exac	rs527236191
Gnomad	rs527236191
Varsome	rs527236191
LitVar	rs527236191
Map	rs527236191
PheGenI	rs527236191
Biobank	rs527236191
1000 genomes	rs527236191
hgdp	rs527236191
ensembl	rs527236191
geneview	rs527236191
scholar	rs527236191
google	rs527236191
pharmgkb	rs527236191
gwascentral	rs527236191
openSNP	rs527236191
23andMe	rs527236191
SNPshot	rs527236191
SNPdbe	rs527236191
MSV3d	rs527236191
GWAS Ctlg	rs527236191

Max Magnitude

0

ClinVar
Risk	rs527236191(G;G)
Alt	rs527236191(G;G)
Reference	Rs527236191(A;A)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	CYTB
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_012920.1:m.15649A>G
CLNSRC	ClinVar
CLNACC	RCV000133435.1,