rs1057521153

Orientation

minus

Stabilized

minus

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

Make rs1057521153(C;C)

Make rs1057521153(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

15456524

Gene

COLQ

is a	snp
is	mentioned by
dbSNP	rs1057521153
dbSNP (classic)	rs1057521153
ClinGen	rs1057521153
ebi	rs1057521153
HLI	rs1057521153
Exac	rs1057521153
Gnomad	rs1057521153
Varsome	rs1057521153
LitVar	rs1057521153
Map	rs1057521153
PheGenI	rs1057521153
Biobank	rs1057521153
1000 genomes	rs1057521153
hgdp	rs1057521153
ensembl	rs1057521153
geneview	rs1057521153
scholar	rs1057521153
google	rs1057521153
pharmgkb	rs1057521153
gwascentral	rs1057521153
openSNP	rs1057521153
23andMe	rs1057521153
SNPshot	rs1057521153
SNPdbe	rs1057521153
MSV3d	rs1057521153
GWAS Ctlg	rs1057521153

Max Magnitude

0

ClinVar
Risk	rs1057521153(C;C)
Alt	rs1057521153(C;C)
Reference	Rs1057521153(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COLQ
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.15498031A>G
CLNSRC
CLNACC	RCV000426405.1,