rs115407852

Orientation

plus

Stabilized

plus

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

Make rs115407852(A;A)

Make rs115407852(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

71681053

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs115407852
dbSNP (classic)	rs115407852
ClinGen	rs115407852
ebi	rs115407852
HLI	rs115407852
Exac	rs115407852
Gnomad	rs115407852
Varsome	rs115407852
LitVar	rs115407852
Map	rs115407852
PheGenI	rs115407852
Biobank	rs115407852
1000 genomes	rs115407852
hgdp	rs115407852
ensembl	rs115407852
geneview	rs115407852
scholar	rs115407852
google	rs115407852
pharmgkb	rs115407852
gwascentral	rs115407852
openSNP	rs115407852
23andMe	rs115407852
SNPshot	rs115407852
SNPdbe	rs115407852
MSV3d	rs115407852
GWAS Ctlg	rs115407852

Max Magnitude

0

ClinVar
Risk	rs115407852(A;A)
Alt	rs115407852(A;A)
Reference	Rs115407852(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	DYSF
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000002.11:g.71908183G>A
CLNSRC
CLNACC	RCV000356385.1, RCV000487973.1,