rs786205511

Orientation

minus

Stabilized

minus

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

Make rs786205511(A;A)

Make rs786205511(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

49097401

Gene

DYM

is a	snp
is	mentioned by
dbSNP	rs786205511
dbSNP (classic)	rs786205511
ClinGen	rs786205511
ebi	rs786205511
HLI	rs786205511
Exac	rs786205511
Gnomad	rs786205511
Varsome	rs786205511
LitVar	rs786205511
Map	rs786205511
PheGenI	rs786205511
Biobank	rs786205511
1000 genomes	rs786205511
hgdp	rs786205511
ensembl	rs786205511
geneview	rs786205511
scholar	rs786205511
google	rs786205511
pharmgkb	rs786205511
gwascentral	rs786205511
openSNP	rs786205511
23andMe	rs786205511
SNPshot	rs786205511
SNPdbe	rs786205511
MSV3d	rs786205511
GWAS Ctlg	rs786205511

Max Magnitude

0

ClinVar
Risk	rs786205511(A;A)
Alt	rs786205511(A;A)
Reference	Rs786205511(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYM
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.46623771C>T
CLNSRC
CLNACC	RCV000171271.1,