rs730880960

Orientation

minus

Stabilized

minus

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

Make rs730880960(C;T)

Make rs730880960(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

46860790

Gene

MYL3

is a	snp
is	mentioned by
dbSNP	rs730880960
dbSNP (classic)	rs730880960
ClinGen	rs730880960
ebi	rs730880960
HLI	rs730880960
Exac	rs730880960
Gnomad	rs730880960
Varsome	rs730880960
LitVar	rs730880960
Map	rs730880960
PheGenI	rs730880960
Biobank	rs730880960
1000 genomes	rs730880960
hgdp	rs730880960
ensembl	rs730880960
geneview	rs730880960
scholar	rs730880960
google	rs730880960
pharmgkb	rs730880960
gwascentral	rs730880960
openSNP	rs730880960
23andMe	rs730880960
SNPshot	rs730880960
SNPdbe	rs730880960
MSV3d	rs730880960
GWAS Ctlg	rs730880960

Max Magnitude

0

ClinVar
Risk	rs730880960(T;T)
Alt	rs730880960(T;T)
Reference	Rs730880960(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYL3
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.46902280G>A
CLNSRC
CLNACC	RCV000158960.1,