rs149701627

Orientation

plus

Stabilized

plus

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

Make rs149701627(C;T)

Make rs149701627(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

7565469

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs149701627
dbSNP (classic)	rs149701627
ClinGen	rs149701627
ebi	rs149701627
HLI	rs149701627
Exac	rs149701627
Gnomad	rs149701627
Varsome	rs149701627
LitVar	rs149701627
Map	rs149701627
PheGenI	rs149701627
Biobank	rs149701627
1000 genomes	rs149701627
hgdp	rs149701627
ensembl	rs149701627
geneview	rs149701627
scholar	rs149701627
google	rs149701627
pharmgkb	rs149701627
gwascentral	rs149701627
openSNP	rs149701627
23andMe	rs149701627
SNPshot	rs149701627
SNPdbe	rs149701627
MSV3d	rs149701627
GWAS Ctlg	rs149701627

Max Magnitude

0

ClinVar
Risk	rs149701627(G;G) rs149701627(T;T)
Alt	rs149701627(G;G) rs149701627(T;T)
Reference	Rs149701627(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSP
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.7565702C>G
CLNSRC
CLNACC	RCV000181280.1,