rs762556795

Orientation

plus

Stabilized

plus

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

Make rs762556795(C;T)

Make rs762556795(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31101968

Gene	DSCAS, DSC2

is a	snp
is	mentioned by
dbSNP	rs762556795
dbSNP (classic)	rs762556795
ClinGen	rs762556795
ebi	rs762556795
HLI	rs762556795
Exac	rs762556795
Gnomad	rs762556795
Varsome	rs762556795
LitVar	rs762556795
Map	rs762556795
PheGenI	rs762556795
Biobank	rs762556795
1000 genomes	rs762556795
hgdp	rs762556795
ensembl	rs762556795
geneview	rs762556795
scholar	rs762556795
google	rs762556795
pharmgkb	rs762556795
gwascentral	rs762556795
openSNP	rs762556795
23andMe	rs762556795
SNPshot	rs762556795
SNPdbe	rs762556795
MSV3d	rs762556795
GWAS Ctlg	rs762556795

Max Magnitude

0

ClinVar
Risk	rs762556795(T;T)
Alt	rs762556795(T;T)
Reference	Rs762556795(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	DSC2 DSCAS LOC101927698
CLNDBN	not specified
Reversed	0
HGVS	NC_000018.9:g.28681931C>T
CLNSRC
CLNACC	RCV000181170.2,