rs770873593

Orientation

plus

Stabilized

plus

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

Make rs770873593(C;T)

Make rs770873593(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

7580388

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs770873593
dbSNP (classic)	rs770873593
ClinGen	rs770873593
ebi	rs770873593
HLI	rs770873593
Exac	rs770873593
Gnomad	rs770873593
Varsome	rs770873593
LitVar	rs770873593
Map	rs770873593
PheGenI	rs770873593
Biobank	rs770873593
1000 genomes	rs770873593
hgdp	rs770873593
ensembl	rs770873593
geneview	rs770873593
scholar	rs770873593
google	rs770873593
pharmgkb	rs770873593
gwascentral	rs770873593
openSNP	rs770873593
23andMe	rs770873593
SNPshot	rs770873593
SNPdbe	rs770873593
MSV3d	rs770873593
GWAS Ctlg	rs770873593

Max Magnitude

0

ClinVar
Risk	rs770873593(T;T)
Alt	rs770873593(T;T)
Reference	Rs770873593(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSP
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.7580621C>T
CLNSRC
CLNACC	RCV000181321.1,