rs863223937

Orientation

minus

Stabilized

minus

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

Make rs863223937(A;C)

Make rs863223937(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

83264308

Gene

COQ2

is a	snp
is	mentioned by
dbSNP	rs863223937
dbSNP (classic)	rs863223937
ClinGen	rs863223937
ebi	rs863223937
HLI	rs863223937
Exac	rs863223937
Gnomad	rs863223937
Varsome	rs863223937
LitVar	rs863223937
Map	rs863223937
PheGenI	rs863223937
Biobank	rs863223937
1000 genomes	rs863223937
hgdp	rs863223937
ensembl	rs863223937
geneview	rs863223937
scholar	rs863223937
google	rs863223937
pharmgkb	rs863223937
gwascentral	rs863223937
openSNP	rs863223937
23andMe	rs863223937
SNPshot	rs863223937
SNPdbe	rs863223937
MSV3d	rs863223937
GWAS Ctlg	rs863223937

Max Magnitude

0

ClinVar
Risk	rs863223937(C;C)
Alt	rs863223937(C;C)
Reference	Rs863223937(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000004.11:g.84185461T>G
CLNSRC
CLNACC	RCV000196578.1,