rs207459996

Orientation

plus

Stabilized

plus

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

Make rs207459996(C;C)

Make rs207459996(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15572

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs207459996
dbSNP (classic)	rs207459996
ClinGen	rs207459996
ebi	rs207459996
HLI	rs207459996
Exac	rs207459996
Gnomad	rs207459996
Varsome	rs207459996
LitVar	rs207459996
Map	rs207459996
PheGenI	rs207459996
Biobank	rs207459996
1000 genomes	rs207459996
hgdp	rs207459996
ensembl	rs207459996
geneview	rs207459996
scholar	rs207459996
google	rs207459996
pharmgkb	rs207459996
gwascentral	rs207459996
openSNP	rs207459996
23andMe	rs207459996
SNPshot	rs207459996
SNPdbe	rs207459996
MSV3d	rs207459996
GWAS Ctlg	rs207459996

Max Magnitude

0

ClinVar
Risk	rs207459996(C;C)
Alt	rs207459996(C;C)
Reference	Rs207459996(T;T)
Significance	Pathogenic
Disease	Familial colorectal cancer
Variation	info
Gene	CYTB
CLNDBN	Familial colorectal cancer
Reversed	0
HGVS	NC_012920.1:m.15572T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010315.4,