rs748363752

Orientation

plus

Stabilized

plus

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

Make rs748363752(A;G)

Make rs748363752(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

49431819

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs748363752
dbSNP (classic)	rs748363752
ClinGen	rs748363752
ebi	rs748363752
HLI	rs748363752
Exac	rs748363752
Gnomad	rs748363752
Varsome	rs748363752
LitVar	rs748363752
Map	rs748363752
PheGenI	rs748363752
Biobank	rs748363752
1000 genomes	rs748363752
hgdp	rs748363752
ensembl	rs748363752
geneview	rs748363752
scholar	rs748363752
google	rs748363752
pharmgkb	rs748363752
gwascentral	rs748363752
openSNP	rs748363752
23andMe	rs748363752
SNPshot	rs748363752
SNPdbe	rs748363752
MSV3d	rs748363752
GWAS Ctlg	rs748363752

Max Magnitude

0

ClinVar
Risk	rs748363752(G;G)
Alt	rs748363752(G;G)
Reference	Rs748363752(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MUT
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.49399532A>T
CLNSRC
CLNACC	RCV000186052.1,