rs786205632

Orientation

plus

Stabilized

plus

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

Make rs786205632(-;-)

Make rs786205632(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

71539192

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs786205632
dbSNP (classic)	rs786205632
ClinGen	rs786205632
ebi	rs786205632
HLI	rs786205632
Exac	rs786205632
Gnomad	rs786205632
Varsome	rs786205632
LitVar	rs786205632
Map	rs786205632
PheGenI	rs786205632
Biobank	rs786205632
1000 genomes	rs786205632
hgdp	rs786205632
ensembl	rs786205632
geneview	rs786205632
scholar	rs786205632
google	rs786205632
pharmgkb	rs786205632
gwascentral	rs786205632
openSNP	rs786205632
23andMe	rs786205632
SNPshot	rs786205632
SNPdbe	rs786205632
MSV3d	rs786205632
GWAS Ctlg	rs786205632

Max Magnitude

0

ClinVar
Risk	rs786205632(-;-)
Alt	rs786205632(-;-)
Reference	Rs786205632(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYSF
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.71766322delC
CLNSRC
CLNACC	RCV000171494.1,