rs527236172

Orientation

plus

Stabilized

plus

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

Make rs527236172(A;G)

Make rs527236172(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15098

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs527236172
dbSNP (classic)	rs527236172
ClinGen	rs527236172
ebi	rs527236172
HLI	rs527236172
Exac	rs527236172
Gnomad	rs527236172
Varsome	rs527236172
LitVar	rs527236172
Map	rs527236172
PheGenI	rs527236172
Biobank	rs527236172
1000 genomes	rs527236172
hgdp	rs527236172
ensembl	rs527236172
geneview	rs527236172
scholar	rs527236172
google	rs527236172
pharmgkb	rs527236172
gwascentral	rs527236172
openSNP	rs527236172
23andMe	rs527236172
SNPshot	rs527236172
SNPdbe	rs527236172
MSV3d	rs527236172
GWAS Ctlg	rs527236172

Max Magnitude

0

ClinVar
Risk	rs527236172(G;G)
Alt	rs527236172(G;G)
Reference	Rs527236172(A;A)
Significance	Probable-Pathogenic
Disease	Neoplasm of ovary
Variation	info
Gene	CYTB
CLNDBN	Neoplasm of ovary
Reversed	0
HGVS	NC_012920.1:m.15098A>G
CLNSRC	ClinVar
CLNACC	RCV000133414.1,