rs143023066

Orientation

plus

Stabilized

plus

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

Make rs143023066(C;T)

Make rs143023066(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

49440273

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs143023066
dbSNP (classic)	rs143023066
ClinGen	rs143023066
ebi	rs143023066
HLI	rs143023066
Exac	rs143023066
Gnomad	rs143023066
Varsome	rs143023066
LitVar	rs143023066
Map	rs143023066
PheGenI	rs143023066
Biobank	rs143023066
1000 genomes	rs143023066
hgdp	rs143023066
ensembl	rs143023066
geneview	rs143023066
scholar	rs143023066
google	rs143023066
pharmgkb	rs143023066
gwascentral	rs143023066
openSNP	rs143023066
23andMe	rs143023066
SNPshot	rs143023066
SNPdbe	rs143023066
MSV3d	rs143023066
GWAS Ctlg	rs143023066

Max Magnitude

0

ClinVar
Risk	rs143023066(T;T)
Alt	rs143023066(T;T)
Reference	Rs143023066(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MUT
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.49407986C>T
CLNSRC
CLNACC	RCV000489642.1,