rs1057519132

Orientation

plus

Stabilized

plus

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

Make rs1057519132(-;-)

Make rs1057519132(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

71664401

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs1057519132
dbSNP (classic)	rs1057519132
ClinGen	rs1057519132
ebi	rs1057519132
HLI	rs1057519132
Exac	rs1057519132
Gnomad	rs1057519132
Varsome	rs1057519132
LitVar	rs1057519132
Map	rs1057519132
PheGenI	rs1057519132
Biobank	rs1057519132
1000 genomes	rs1057519132
hgdp	rs1057519132
ensembl	rs1057519132
geneview	rs1057519132
scholar	rs1057519132
google	rs1057519132
pharmgkb	rs1057519132
gwascentral	rs1057519132
openSNP	rs1057519132
23andMe	rs1057519132
SNPshot	rs1057519132
SNPdbe	rs1057519132
MSV3d	rs1057519132
GWAS Ctlg	rs1057519132

Max Magnitude

0

ClinVar
Risk	rs1057519132(-;-)
Alt	rs1057519132(-;-)
Reference	Rs1057519132(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYSF
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.71891531delT
CLNSRC
CLNACC	RCV000416117.2,