rs193302996

Orientation

plus

Stabilized

plus

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

Make rs193302996(A;G)

Make rs193302996(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15607

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs193302996
dbSNP (classic)	rs193302996
ClinGen	rs193302996
ebi	rs193302996
HLI	rs193302996
Exac	rs193302996
Gnomad	rs193302996
Varsome	rs193302996
LitVar	rs193302996
Map	rs193302996
PheGenI	rs193302996
Biobank	rs193302996
1000 genomes	rs193302996
hgdp	rs193302996
ensembl	rs193302996
geneview	rs193302996
scholar	rs193302996
google	rs193302996
pharmgkb	rs193302996
gwascentral	rs193302996
openSNP	rs193302996
23andMe	rs193302996
SNPshot	rs193302996
SNPdbe	rs193302996
MSV3d	rs193302996
GWAS Ctlg	rs193302996

Max Magnitude

0

ClinVar
Risk	rs193302996(G;G)
Alt	rs193302996(G;G)
Reference	Rs193302996(A;A)
Significance	Probable-Pathogenic
Disease	Neoplasm of ovary
Variation	info
Gene	CYTB
CLNDBN	Neoplasm of ovary
Reversed	0
HGVS	NC_012920.1:m.15607A>G
CLNSRC
CLNACC	RCV000133457.1,