rs199474706

Orientation

minus

Stabilized

minus

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

Make rs199474706(C;G)

Make rs199474706(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46859493

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs199474706
dbSNP (classic)	rs199474706
ClinGen	rs199474706
ebi	rs199474706
HLI	rs199474706
Exac	rs199474706
Gnomad	rs199474706
Varsome	rs199474706
LitVar	rs199474706
Map	rs199474706
PheGenI	rs199474706
Biobank	rs199474706
1000 genomes	rs199474706
hgdp	rs199474706
ensembl	rs199474706
geneview	rs199474706
scholar	rs199474706
google	rs199474706
pharmgkb	rs199474706
gwascentral	rs199474706
openSNP	rs199474706
23andMe	rs199474706
SNPshot	rs199474706
SNPdbe	rs199474706
MSV3d	rs199474706
GWAS Ctlg	rs199474706

Max Magnitude

0

ClinVar
Risk	rs199474706(G;G)
Alt	rs199474706(G;G)
Reference	Rs199474706(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MYL3
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.46900983G>C
CLNSRC	Leiden Muscular Dystrophy pages (MYL3)
CLNACC	RCV000024474.2,