rs207459995

Orientation

plus

Stabilized

plus

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

Make rs207459995(A;A)

Make rs207459995(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14985

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs207459995
dbSNP (classic)	rs207459995
ClinGen	rs207459995
ebi	rs207459995
HLI	rs207459995
Exac	rs207459995
Gnomad	rs207459995
Varsome	rs207459995
LitVar	rs207459995
Map	rs207459995
PheGenI	rs207459995
Biobank	rs207459995
1000 genomes	rs207459995
hgdp	rs207459995
ensembl	rs207459995
geneview	rs207459995
scholar	rs207459995
google	rs207459995
pharmgkb	rs207459995
gwascentral	rs207459995
openSNP	rs207459995
23andMe	rs207459995
SNPshot	rs207459995
SNPdbe	rs207459995
MSV3d	rs207459995
GWAS Ctlg	rs207459995

Max Magnitude

0

ClinVar
Risk	rs207459995(A;A)
Alt	rs207459995(A;A)
Reference	Rs207459995(G;G)
Significance	Pathogenic
Disease	Familial colorectal cancer
Variation	info
Gene	CYTB
CLNDBN	Familial colorectal cancer
Reversed	0
HGVS	NC_012920.1:m.14985G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010314.2,