rs138268837

Orientation

plus

Stabilized

plus

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

Make rs138268837(C;G)

Make rs138268837(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

71612672

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs138268837
dbSNP (classic)	rs138268837
ClinGen	rs138268837
ebi	rs138268837
HLI	rs138268837
Exac	rs138268837
Gnomad	rs138268837
Varsome	rs138268837
LitVar	rs138268837
Map	rs138268837
PheGenI	rs138268837
Biobank	rs138268837
1000 genomes	rs138268837
hgdp	rs138268837
ensembl	rs138268837
geneview	rs138268837
scholar	rs138268837
google	rs138268837
pharmgkb	rs138268837
gwascentral	rs138268837
openSNP	rs138268837
23andMe	rs138268837
SNPshot	rs138268837
SNPdbe	rs138268837
MSV3d	rs138268837
GWAS Ctlg	rs138268837

Max Magnitude

0

ClinVar
Risk	rs138268837(A;A) rs138268837(G;G)
Alt	rs138268837(A;A) rs138268837(G;G)
Reference	Rs138268837(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DYSF
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.71839802C>G
CLNSRC
CLNACC	RCV000494287.1,