rs779212460

Orientation

plus

Stabilized

plus

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

Make rs779212460(C;T)

Make rs779212460(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

123725955

Gene

MYLK

is a	snp
is	mentioned by
dbSNP	rs779212460
dbSNP (classic)	rs779212460
ClinGen	rs779212460
ebi	rs779212460
HLI	rs779212460
Exac	rs779212460
Gnomad	rs779212460
Varsome	rs779212460
LitVar	rs779212460
Map	rs779212460
PheGenI	rs779212460
Biobank	rs779212460
1000 genomes	rs779212460
hgdp	rs779212460
ensembl	rs779212460
geneview	rs779212460
scholar	rs779212460
google	rs779212460
pharmgkb	rs779212460
gwascentral	rs779212460
openSNP	rs779212460
23andMe	rs779212460
SNPshot	rs779212460
SNPdbe	rs779212460
MSV3d	rs779212460
GWAS Ctlg	rs779212460

Max Magnitude

0

ClinVar
Risk	rs779212460(T;T)
Alt	rs779212460(T;T)
Reference	Rs779212460(C;C)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYLK
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.123444802C>T
CLNSRC
CLNACC	RCV000182570.2,