rs1057521141

Orientation

plus

Stabilized

plus

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

Make rs1057521141(C;T)

Make rs1057521141(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

71679197

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs1057521141
dbSNP (classic)	rs1057521141
ClinGen	rs1057521141
ebi	rs1057521141
HLI	rs1057521141
Exac	rs1057521141
Gnomad	rs1057521141
Varsome	rs1057521141
LitVar	rs1057521141
Map	rs1057521141
PheGenI	rs1057521141
Biobank	rs1057521141
1000 genomes	rs1057521141
hgdp	rs1057521141
ensembl	rs1057521141
geneview	rs1057521141
scholar	rs1057521141
google	rs1057521141
pharmgkb	rs1057521141
gwascentral	rs1057521141
openSNP	rs1057521141
23andMe	rs1057521141
SNPshot	rs1057521141
SNPdbe	rs1057521141
MSV3d	rs1057521141
GWAS Ctlg	rs1057521141

Max Magnitude

0

ClinVar
Risk	rs1057521141(T;T)
Alt	rs1057521141(T;T)
Reference	Rs1057521141(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYSF
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.71906327C>T
CLNSRC
CLNACC	RCV000424011.1,