rs527236195

Orientation

plus

Stabilized

plus

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

Make rs527236195(A;A)

Make rs527236195(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15884

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs527236195
dbSNP (classic)	rs527236195
ClinGen	rs527236195
ebi	rs527236195
HLI	rs527236195
Exac	rs527236195
Gnomad	rs527236195
Varsome	rs527236195
LitVar	rs527236195
Map	rs527236195
PheGenI	rs527236195
Biobank	rs527236195
1000 genomes	rs527236195
hgdp	rs527236195
ensembl	rs527236195
geneview	rs527236195
scholar	rs527236195
google	rs527236195
pharmgkb	rs527236195
gwascentral	rs527236195
openSNP	rs527236195
23andMe	rs527236195
SNPshot	rs527236195
SNPdbe	rs527236195
MSV3d	rs527236195
GWAS Ctlg	rs527236195

Merged from

Rs28617642

Max Magnitude

0

ClinVar
Risk	rs527236195(A;A) rs527236195(C;C)
Alt	rs527236195(A;A) rs527236195(C;C)
Reference	Rs527236195(G;G)
Significance	Probable-Pathogenic
Disease	Neoplasm of ovary not specified
Variation	info
Gene	CYTB
CLNDBN	Neoplasm of ovary not specified
Reversed	0
HGVS	NC_012920.1:m.15884G>A; NC_012920.1:m.15884G>C
CLNSRC	ClinVar
CLNACC	RCV000133439.1, RCV000238892.1,