rs794728985

Orientation

plus

Stabilized

plus

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

Make rs794728985(C;T)

Make rs794728985(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

219420591

Gene

DES

is a	snp
is	mentioned by
dbSNP	rs794728985
dbSNP (classic)	rs794728985
ClinGen	rs794728985
ebi	rs794728985
HLI	rs794728985
Exac	rs794728985
Gnomad	rs794728985
Varsome	rs794728985
LitVar	rs794728985
Map	rs794728985
PheGenI	rs794728985
Biobank	rs794728985
1000 genomes	rs794728985
hgdp	rs794728985
ensembl	rs794728985
geneview	rs794728985
scholar	rs794728985
google	rs794728985
pharmgkb	rs794728985
gwascentral	rs794728985
openSNP	rs794728985
23andMe	rs794728985
SNPshot	rs794728985
SNPdbe	rs794728985
MSV3d	rs794728985
GWAS Ctlg	rs794728985

Max Magnitude

0

ClinVar
Risk	rs794728985(T;T)
Alt	rs794728985(T;T)
Reference	Rs794728985(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	DES
CLNDBN	not specified
Reversed	0
HGVS	NC_000002.11:g.220285313C>T
CLNSRC
CLNACC	RCV000183349.2,