rs267607498

Orientation

plus

Stabilized

plus

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

Make rs267607498(A;G)

Make rs267607498(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

219425707

Gene

DES

is a	snp
is	mentioned by
dbSNP	rs267607498
dbSNP (classic)	rs267607498
ClinGen	rs267607498
ebi	rs267607498
HLI	rs267607498
Exac	rs267607498
Gnomad	rs267607498
Varsome	rs267607498
LitVar	rs267607498
Map	rs267607498
PheGenI	rs267607498
Biobank	rs267607498
1000 genomes	rs267607498
hgdp	rs267607498
ensembl	rs267607498
geneview	rs267607498
scholar	rs267607498
google	rs267607498
pharmgkb	rs267607498
gwascentral	rs267607498
openSNP	rs267607498
23andMe	rs267607498
SNPshot	rs267607498
SNPdbe	rs267607498
MSV3d	rs267607498
GWAS Ctlg	rs267607498

Max Magnitude

0

ClinVar
Risk	rs267607498(G;G)
Alt	rs267607498(G;G)
Reference	Rs267607498(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DES LOC101928568
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.220290429A>G
CLNSRC
CLNACC	RCV000056785.2,