rs777031588

Orientation

plus

Stabilized

plus

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

Make rs777031588(C;C)

Make rs777031588(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

49451724

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs777031588
dbSNP (classic)	rs777031588
ClinGen	rs777031588
ebi	rs777031588
HLI	rs777031588
Exac	rs777031588
Gnomad	rs777031588
Varsome	rs777031588
LitVar	rs777031588
Map	rs777031588
PheGenI	rs777031588
Biobank	rs777031588
1000 genomes	rs777031588
hgdp	rs777031588
ensembl	rs777031588
geneview	rs777031588
scholar	rs777031588
google	rs777031588
pharmgkb	rs777031588
gwascentral	rs777031588
openSNP	rs777031588
23andMe	rs777031588
SNPshot	rs777031588
SNPdbe	rs777031588
MSV3d	rs777031588
GWAS Ctlg	rs777031588

Max Magnitude

0

ClinVar
Risk	rs777031588(C;C)
Alt	rs777031588(C;C)
Reference	Rs777031588(T;T)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MUT
CLNDBN	not specified
Reversed	0
HGVS	NC_000006.11:g.49419437T>C
CLNSRC
CLNACC	RCV000186045.2,