rs141026028

Orientation

plus

Stabilized

plus

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

Make rs141026028(A;A)

Make rs141026028(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

7583758

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs141026028
dbSNP (classic)	rs141026028
ClinGen	rs141026028
ebi	rs141026028
HLI	rs141026028
Exac	rs141026028
Gnomad	rs141026028
Varsome	rs141026028
LitVar	rs141026028
Map	rs141026028
PheGenI	rs141026028
Biobank	rs141026028
1000 genomes	rs141026028
hgdp	rs141026028
ensembl	rs141026028
geneview	rs141026028
scholar	rs141026028
google	rs141026028
pharmgkb	rs141026028
gwascentral	rs141026028
openSNP	rs141026028
23andMe	rs141026028
SNPshot	rs141026028
SNPdbe	rs141026028
MSV3d	rs141026028
GWAS Ctlg	rs141026028

Max Magnitude

0

ClinVar
Risk	rs141026028(A;A) rs141026028(T;T)
Alt	rs141026028(A;A) rs141026028(T;T)
Reference	Rs141026028(C;C)
Significance	Pathogenic
Disease	Cardiovascular phenotype not provided
Variation	info
Gene	DSP
CLNDBN	Cardiovascular phenotype not provided
Reversed	0
HGVS	NC_000006.11:g.7583991C>A; NC_000006.11:g.7583991C>T
CLNSRC
CLNACC	RCV000243168.1, RCV000181342.2,