rs886039128

Orientation

minus

Stabilized

minus

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

Make rs886039128(A;A)

Make rs886039128(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

18

Position

31079990

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs886039128
dbSNP (classic)	rs886039128
ClinGen	rs886039128
ebi	rs886039128
HLI	rs886039128
Exac	rs886039128
Gnomad	rs886039128
Varsome	rs886039128
LitVar	rs886039128
Map	rs886039128
PheGenI	rs886039128
Biobank	rs886039128
1000 genomes	rs886039128
hgdp	rs886039128
ensembl	rs886039128
geneview	rs886039128
scholar	rs886039128
google	rs886039128
pharmgkb	rs886039128
gwascentral	rs886039128
openSNP	rs886039128
23andMe	rs886039128
SNPshot	rs886039128
SNPdbe	rs886039128
MSV3d	rs886039128
GWAS Ctlg	rs886039128

Max Magnitude

0

ClinVar
Risk	rs886039128(A;A)
Alt	rs886039128(A;A)
Reference	Rs886039128(G;G)
Significance	Probable-Pathogenic
Disease	Cardiovascular phenotype
Variation	info
Gene	DSC2
CLNDBN	Cardiovascular phenotype
Reversed	1
HGVS	NC_000018.9:g.28659956C>T
CLNSRC
CLNACC	RCV000246983.1,