rs794728112

Orientation

plus

Stabilized

plus

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

Make rs794728112(A;T)

Make rs794728112(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

7567411

Gene

DSP

is a	snp
is	mentioned by
dbSNP	rs794728112
dbSNP (classic)	rs794728112
ClinGen	rs794728112
ebi	rs794728112
HLI	rs794728112
Exac	rs794728112
Gnomad	rs794728112
Varsome	rs794728112
LitVar	rs794728112
Map	rs794728112
PheGenI	rs794728112
Biobank	rs794728112
1000 genomes	rs794728112
hgdp	rs794728112
ensembl	rs794728112
geneview	rs794728112
scholar	rs794728112
google	rs794728112
pharmgkb	rs794728112
gwascentral	rs794728112
openSNP	rs794728112
23andMe	rs794728112
SNPshot	rs794728112
SNPdbe	rs794728112
MSV3d	rs794728112
GWAS Ctlg	rs794728112

Max Magnitude

0

ClinVar
Risk	rs794728112(G;G) rs794728112(T;T)
Alt	rs794728112(G;G) rs794728112(T;T)
Reference	Rs794728112(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	DSP
CLNDBN	not specified
Reversed	0
HGVS	NC_000006.11:g.7567644A>G; NC_000006.11:g.7567644A>T
CLNSRC
CLNACC	RCV000486549.1, RCV000181286.2,