rs863223942

Orientation

minus

Stabilized

minus

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

Make rs863223942(C;C)

Make rs863223942(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

99714639

Gene

COX15

is a	snp
is	mentioned by
dbSNP	rs863223942
dbSNP (classic)	rs863223942
ClinGen	rs863223942
ebi	rs863223942
HLI	rs863223942
Exac	rs863223942
Gnomad	rs863223942
Varsome	rs863223942
LitVar	rs863223942
Map	rs863223942
PheGenI	rs863223942
Biobank	rs863223942
1000 genomes	rs863223942
hgdp	rs863223942
ensembl	rs863223942
geneview	rs863223942
scholar	rs863223942
google	rs863223942
pharmgkb	rs863223942
gwascentral	rs863223942
openSNP	rs863223942
23andMe	rs863223942
SNPshot	rs863223942
SNPdbe	rs863223942
MSV3d	rs863223942
GWAS Ctlg	rs863223942

Max Magnitude

0

ClinVar
Risk	rs863223942(C;C)
Alt	rs863223942(C;C)
Reference	Rs863223942(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COX15
CLNDBN	not provided
Reversed	1
HGVS	NC_000010.10:g.101474396A>G
CLNSRC
CLNACC	RCV000199309.1,