rs766420051

Orientation

plus

Stabilized

plus

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

Make rs766420051(C;G)

Make rs766420051(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

49456165

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs766420051
dbSNP (classic)	rs766420051
ClinGen	rs766420051
ebi	rs766420051
HLI	rs766420051
Exac	rs766420051
Gnomad	rs766420051
Varsome	rs766420051
LitVar	rs766420051
Map	rs766420051
PheGenI	rs766420051
Biobank	rs766420051
1000 genomes	rs766420051
hgdp	rs766420051
ensembl	rs766420051
geneview	rs766420051
scholar	rs766420051
google	rs766420051
pharmgkb	rs766420051
gwascentral	rs766420051
openSNP	rs766420051
23andMe	rs766420051
SNPshot	rs766420051
SNPdbe	rs766420051
MSV3d	rs766420051
GWAS Ctlg	rs766420051

Max Magnitude

0

ClinVar
Risk	rs766420051(G;G)
Alt	rs766420051(G;G)
Reference	Rs766420051(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MUT
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.49423878C>A
CLNSRC
CLNACC	RCV000186058.1,