rs786205524

Orientation

plus

Stabilized

plus

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

Make rs786205524(A;A)

Make rs786205524(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

71480882

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs786205524
dbSNP (classic)	rs786205524
ClinGen	rs786205524
ebi	rs786205524
HLI	rs786205524
Exac	rs786205524
Gnomad	rs786205524
Varsome	rs786205524
LitVar	rs786205524
Map	rs786205524
PheGenI	rs786205524
Biobank	rs786205524
1000 genomes	rs786205524
hgdp	rs786205524
ensembl	rs786205524
geneview	rs786205524
scholar	rs786205524
google	rs786205524
pharmgkb	rs786205524
gwascentral	rs786205524
openSNP	rs786205524
23andMe	rs786205524
SNPshot	rs786205524
SNPdbe	rs786205524
MSV3d	rs786205524
GWAS Ctlg	rs786205524

Max Magnitude

0

ClinVar
Risk	rs786205524(A;A)
Alt	rs786205524(A;A)
Reference	Rs786205524(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYSF
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.71708012G>A
CLNSRC
CLNACC	RCV000171291.1,