rs727504020

Orientation

minus

Stabilized

minus

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

Make rs727504020(C;T)

Make rs727504020(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

49451591

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs727504020
dbSNP (classic)	rs727504020
ClinGen	rs727504020
ebi	rs727504020
HLI	rs727504020
Exac	rs727504020
Gnomad	rs727504020
Varsome	rs727504020
LitVar	rs727504020
Map	rs727504020
PheGenI	rs727504020
Biobank	rs727504020
1000 genomes	rs727504020
hgdp	rs727504020
ensembl	rs727504020
geneview	rs727504020
scholar	rs727504020
google	rs727504020
pharmgkb	rs727504020
gwascentral	rs727504020
openSNP	rs727504020
23andMe	rs727504020
SNPshot	rs727504020
SNPdbe	rs727504020
MSV3d	rs727504020
GWAS Ctlg	rs727504020

Max Magnitude

0

ClinVar
Risk	rs727504020(G;G) rs727504020(T;T)
Alt	rs727504020(G;G) rs727504020(T;T)
Reference	Rs727504020(C;C)
Significance	Pathogenic
Disease	not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Variation	info
Gene	MUT
CLNDBN	not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Reversed	1
HGVS	NC_000006.11:g.49419304G>A
CLNSRC	HGMD
CLNACC	RCV000153520.2, RCV000179277.2,