rs199474708

Orientation

minus

Stabilized

minus

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

Make rs199474708(A;G)

Make rs199474708(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46858426

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs199474708
dbSNP (classic)	rs199474708
ClinGen	rs199474708
ebi	rs199474708
HLI	rs199474708
Exac	rs199474708
Gnomad	rs199474708
Varsome	rs199474708
LitVar	rs199474708
Map	rs199474708
PheGenI	rs199474708
Biobank	rs199474708
1000 genomes	rs199474708
hgdp	rs199474708
ensembl	rs199474708
geneview	rs199474708
scholar	rs199474708
google	rs199474708
pharmgkb	rs199474708
gwascentral	rs199474708
openSNP	rs199474708
23andMe	rs199474708
SNPshot	rs199474708
SNPdbe	rs199474708
MSV3d	rs199474708
GWAS Ctlg	rs199474708

Max Magnitude

0

ClinVar
Risk	rs199474708(G;G)
Alt	rs199474708(G;G)
Reference	Rs199474708(A;A)
Significance	Untested
Disease	not provided not specified
Variation	info
Gene	MYL3
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000003.11:g.46899916T>C
CLNSRC	Leiden Muscular Dystrophy pages (MYL3)
CLNACC	RCV000024470.1, RCV000036029.3,