rs567723663

Orientation

plus

Stabilized

plus

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

Make rs567723663(C;C)

Make rs567723663(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46858471

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs567723663
dbSNP (classic)	rs567723663
ClinGen	rs567723663
ebi	rs567723663
HLI	rs567723663
Exac	rs567723663
Gnomad	rs567723663
Varsome	rs567723663
LitVar	rs567723663
Map	rs567723663
PheGenI	rs567723663
Biobank	rs567723663
1000 genomes	rs567723663
hgdp	rs567723663
ensembl	rs567723663
geneview	rs567723663
scholar	rs567723663
google	rs567723663
pharmgkb	rs567723663
gwascentral	rs567723663
openSNP	rs567723663
23andMe	rs567723663
SNPshot	rs567723663
SNPdbe	rs567723663
MSV3d	rs567723663
GWAS Ctlg	rs567723663

Max Magnitude

0

ClinVar
Risk	rs567723663(A;A) rs567723663(C;C)
Alt	rs567723663(A;A) rs567723663(C;C)
Reference	Rs567723663(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYL3
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.46899961G>A
CLNSRC
CLNACC	RCV000171360.1,