rs368918847

Orientation

plus

Stabilized

plus

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

Make rs368918847(C;T)

Make rs368918847(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

14207106

Gene

COX10

is a	snp
is	mentioned by
dbSNP	rs368918847
dbSNP (classic)	rs368918847
ClinGen	rs368918847
ebi	rs368918847
HLI	rs368918847
Exac	rs368918847
Gnomad	rs368918847
Varsome	rs368918847
LitVar	rs368918847
Map	rs368918847
PheGenI	rs368918847
Biobank	rs368918847
1000 genomes	rs368918847
hgdp	rs368918847
ensembl	rs368918847
geneview	rs368918847
scholar	rs368918847
google	rs368918847
pharmgkb	rs368918847
gwascentral	rs368918847
openSNP	rs368918847
23andMe	rs368918847
SNPshot	rs368918847
SNPdbe	rs368918847
MSV3d	rs368918847
GWAS Ctlg	rs368918847

Max Magnitude

0

ClinVar
Risk	rs368918847(A;A) rs368918847(T;T)
Alt	rs368918847(A;A) rs368918847(T;T)
Reference	Rs368918847(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COX10
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.14110423C>T
CLNSRC
CLNACC	RCV000479216.1,