rs763903197

Orientation

plus

Stabilized

plus

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

Make rs763903197(A;A)

Make rs763903197(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

219421343

Gene

DES

is a	snp
is	mentioned by
dbSNP	rs763903197
dbSNP (classic)	rs763903197
ClinGen	rs763903197
ebi	rs763903197
HLI	rs763903197
Exac	rs763903197
Gnomad	rs763903197
Varsome	rs763903197
LitVar	rs763903197
Map	rs763903197
PheGenI	rs763903197
Biobank	rs763903197
1000 genomes	rs763903197
hgdp	rs763903197
ensembl	rs763903197
geneview	rs763903197
scholar	rs763903197
google	rs763903197
pharmgkb	rs763903197
gwascentral	rs763903197
openSNP	rs763903197
23andMe	rs763903197
SNPshot	rs763903197
SNPdbe	rs763903197
MSV3d	rs763903197
GWAS Ctlg	rs763903197

Max Magnitude

0

ClinVar
Risk	rs763903197(A;A)
Alt	rs763903197(A;A)
Reference	Rs763903197(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	DES
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000002.11:g.220286065G>A
CLNSRC
CLNACC	RCV000183353.2, RCV000278818.1,