rs199870606

Orientation

plus

Stabilized

plus

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

Make rs199870606(C;T)

Make rs199870606(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

71611483

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs199870606
dbSNP (classic)	rs199870606
ClinGen	rs199870606
ebi	rs199870606
HLI	rs199870606
Exac	rs199870606
Gnomad	rs199870606
Varsome	rs199870606
LitVar	rs199870606
Map	rs199870606
PheGenI	rs199870606
Biobank	rs199870606
1000 genomes	rs199870606
hgdp	rs199870606
ensembl	rs199870606
geneview	rs199870606
scholar	rs199870606
google	rs199870606
pharmgkb	rs199870606
gwascentral	rs199870606
openSNP	rs199870606
23andMe	rs199870606
SNPshot	rs199870606
SNPdbe	rs199870606
MSV3d	rs199870606
GWAS Ctlg	rs199870606

Max Magnitude

0

ClinVar
Risk	rs199870606(T;T)
Alt	rs199870606(T;T)
Reference	Rs199870606(C;C)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	DYSF
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000002.11:g.71838613C>T
CLNSRC
CLNACC	RCV000343658.2, RCV000408314.1,