rs761785906

Orientation

plus

Stabilized

plus

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

Make rs761785906(A;A)

Make rs761785906(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

83267737

Gene

COQ2

is a	snp
is	mentioned by
dbSNP	rs761785906
dbSNP (classic)	rs761785906
ClinGen	rs761785906
ebi	rs761785906
HLI	rs761785906
Exac	rs761785906
Gnomad	rs761785906
Varsome	rs761785906
LitVar	rs761785906
Map	rs761785906
PheGenI	rs761785906
Biobank	rs761785906
1000 genomes	rs761785906
hgdp	rs761785906
ensembl	rs761785906
geneview	rs761785906
scholar	rs761785906
google	rs761785906
pharmgkb	rs761785906
gwascentral	rs761785906
openSNP	rs761785906
23andMe	rs761785906
SNPshot	rs761785906
SNPdbe	rs761785906
MSV3d	rs761785906
GWAS Ctlg	rs761785906

Max Magnitude

0

ClinVar
Risk	rs761785906(A;A)
Alt	rs761785906(A;A)
Reference	Rs761785906(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	COQ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.84188890G>A
CLNSRC
CLNACC	RCV000195593.1,