rs794728145

Orientation

plus

Stabilized

plus

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

Make rs794728145(ACAGCGCC;GTG)

Make rs794728145(GTG;GTG)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

7582812

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs794728145
dbSNP (classic)	rs794728145
ClinGen	rs794728145
ebi	rs794728145
HLI	rs794728145
Exac	rs794728145
Gnomad	rs794728145
Varsome	rs794728145
LitVar	rs794728145
Map	rs794728145
PheGenI	rs794728145
Biobank	rs794728145
1000 genomes	rs794728145
hgdp	rs794728145
ensembl	rs794728145
geneview	rs794728145
scholar	rs794728145
google	rs794728145
pharmgkb	rs794728145
gwascentral	rs794728145
openSNP	rs794728145
23andMe	rs794728145
SNPshot	rs794728145
SNPdbe	rs794728145
MSV3d	rs794728145
GWAS Ctlg	rs794728145

Max Magnitude

0

ClinVar
Risk	rs794728145(GTG;GTG)
Alt	rs794728145(GTG;GTG)
Reference	Rs794728145(ACAGCGCC;ACAGCGCC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSP
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.7583045_7583052delACAGCGCCinsGTG
CLNSRC
CLNACC	RCV000181368.1,