rs369511505

Orientation

plus

Stabilized

plus

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

Make rs369511505(C;T)

Make rs369511505(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

14077002

Gene

COX10

is a	snp
is	mentioned by
dbSNP	rs369511505
dbSNP (classic)	rs369511505
ClinGen	rs369511505
ebi	rs369511505
HLI	rs369511505
Exac	rs369511505
Gnomad	rs369511505
Varsome	rs369511505
LitVar	rs369511505
Map	rs369511505
PheGenI	rs369511505
Biobank	rs369511505
1000 genomes	rs369511505
hgdp	rs369511505
ensembl	rs369511505
geneview	rs369511505
scholar	rs369511505
google	rs369511505
pharmgkb	rs369511505
gwascentral	rs369511505
openSNP	rs369511505
23andMe	rs369511505
SNPshot	rs369511505
SNPdbe	rs369511505
MSV3d	rs369511505
GWAS Ctlg	rs369511505

Max Magnitude

0

ClinVar
Risk	rs369511505(T;T)
Alt	rs369511505(T;T)
Reference	Rs369511505(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COX10
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.13980319C>T
CLNSRC
CLNACC	RCV000494123.1,