rs796756333

Orientation

plus

Stabilized

plus

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

Make rs796756333(C;T)

Make rs796756333(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

31083061

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs796756333
dbSNP (classic)	rs796756333
ClinGen	rs796756333
ebi	rs796756333
HLI	rs796756333
Exac	rs796756333
Gnomad	rs796756333
Varsome	rs796756333
LitVar	rs796756333
Map	rs796756333
PheGenI	rs796756333
Biobank	rs796756333
1000 genomes	rs796756333
hgdp	rs796756333
ensembl	rs796756333
geneview	rs796756333
scholar	rs796756333
google	rs796756333
pharmgkb	rs796756333
gwascentral	rs796756333
openSNP	rs796756333
23andMe	rs796756333
SNPshot	rs796756333
SNPdbe	rs796756333
MSV3d	rs796756333
GWAS Ctlg	rs796756333

Max Magnitude

0

ClinVar
Risk	rs796756333(T;T)
Alt	rs796756333(T;T)
Reference	Rs796756333(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DSC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.28663027C>T
CLNSRC
CLNACC	RCV000484445.1,