rs886044183

Orientation

plus

Stabilized

plus

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

Chromosome

19

Position

46756420

Gene

FKRP

is a	snp
is	mentioned by
dbSNP	rs886044183
dbSNP (classic)	rs886044183
ClinGen	rs886044183
ebi	rs886044183
HLI	rs886044183
Exac	rs886044183
Gnomad	rs886044183
Varsome	rs886044183
LitVar	rs886044183
Map	rs886044183
PheGenI	rs886044183
Biobank	rs886044183
1000 genomes	rs886044183
hgdp	rs886044183
ensembl	rs886044183
geneview	rs886044183
scholar	rs886044183
google	rs886044183
pharmgkb	rs886044183
gwascentral	rs886044183
openSNP	rs886044183
23andMe	rs886044183
SNPshot	rs886044183
SNPdbe	rs886044183
MSV3d	rs886044183
GWAS Ctlg	rs886044183

Max Magnitude

0

ClinVar
Risk	rs886044183(T;T)
Alt	rs886044183(T;T)
Reference	Rs886044183(G;G)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy-dystroglycanopathy Walker-Warburg congenital muscular dystrophy
Variation	info
Gene	FKRP
CLNDBN	Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Walker-Warburg congenital muscular dystrophy
Reversed	0
HGVS	NC_000019.9:g.47259677G>T
CLNSRC
CLNACC	RCV000282481.1, RCV000461986.1,