rs796052002

Orientation

minus

Stabilized

minus

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

Make rs796052002(C;T)

Make rs796052002(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

49453686

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs796052002
dbSNP (classic)	rs796052002
ClinGen	rs796052002
ebi	rs796052002
HLI	rs796052002
Exac	rs796052002
Gnomad	rs796052002
Varsome	rs796052002
LitVar	rs796052002
Map	rs796052002
PheGenI	rs796052002
Biobank	rs796052002
1000 genomes	rs796052002
hgdp	rs796052002
ensembl	rs796052002
geneview	rs796052002
scholar	rs796052002
google	rs796052002
pharmgkb	rs796052002
gwascentral	rs796052002
openSNP	rs796052002
23andMe	rs796052002
SNPshot	rs796052002
SNPdbe	rs796052002
MSV3d	rs796052002
GWAS Ctlg	rs796052002

Max Magnitude

0

ClinVar
Risk	rs796052002(T;T)
Alt	rs796052002(T;T)
Reference	Rs796052002(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MUT
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.49421399G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186044.1,