rs786205525

Orientation

plus

Stabilized

plus

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

Make rs786205525(A;G)

Make rs786205525(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

71513889

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs786205525
dbSNP (classic)	rs786205525
ClinGen	rs786205525
ebi	rs786205525
HLI	rs786205525
Exac	rs786205525
Gnomad	rs786205525
Varsome	rs786205525
LitVar	rs786205525
Map	rs786205525
PheGenI	rs786205525
Biobank	rs786205525
1000 genomes	rs786205525
hgdp	rs786205525
ensembl	rs786205525
geneview	rs786205525
scholar	rs786205525
google	rs786205525
pharmgkb	rs786205525
gwascentral	rs786205525
openSNP	rs786205525
23andMe	rs786205525
SNPshot	rs786205525
SNPdbe	rs786205525
MSV3d	rs786205525
GWAS Ctlg	rs786205525

Max Magnitude

0

ClinVar
Risk	rs786205525(G;G)
Alt	rs786205525(G;G)
Reference	Rs786205525(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYSF
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.71741019A>G
CLNSRC
CLNACC	RCV000171292.1,