rs199474705

Orientation

minus

Stabilized

minus

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

Make rs199474705(A;A)

Make rs199474705(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

46859502

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs199474705
dbSNP (classic)	rs199474705
ClinGen	rs199474705
ebi	rs199474705
HLI	rs199474705
Exac	rs199474705
Gnomad	rs199474705
Varsome	rs199474705
LitVar	rs199474705
Map	rs199474705
PheGenI	rs199474705
Biobank	rs199474705
1000 genomes	rs199474705
hgdp	rs199474705
ensembl	rs199474705
geneview	rs199474705
scholar	rs199474705
google	rs199474705
pharmgkb	rs199474705
gwascentral	rs199474705
openSNP	rs199474705
23andMe	rs199474705
SNPshot	rs199474705
SNPdbe	rs199474705
MSV3d	rs199474705
GWAS Ctlg	rs199474705

Max Magnitude

0

ClinVar
Risk	rs199474705(A;A)
Alt	rs199474705(A;A)
Reference	Rs199474705(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYL3
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.46900992C>T
CLNSRC	Leiden Muscular Dystrophy pages (MYL3)
CLNACC	RCV000024473.1,