rs121913580

Orientation

plus

Stabilized

plus

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

Make rs121913580(C;T)

Make rs121913580(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

236852578

Gene

MTR

is a	snp
is	mentioned by
dbSNP	rs121913580
dbSNP (classic)	rs121913580
ClinGen	rs121913580
ebi	rs121913580
HLI	rs121913580
Exac	rs121913580
Gnomad	rs121913580
Varsome	rs121913580
LitVar	rs121913580
Map	rs121913580
PheGenI	rs121913580
Biobank	rs121913580
1000 genomes	rs121913580
hgdp	rs121913580
ensembl	rs121913580
geneview	rs121913580
scholar	rs121913580
google	rs121913580
pharmgkb	rs121913580
gwascentral	rs121913580
openSNP	rs121913580
23andMe	rs121913580
SNPshot	rs121913580
SNPdbe	rs121913580
MSV3d	rs121913580
GWAS Ctlg	rs121913580

Max Magnitude

0

OMIM	156570
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121913580(T;T)
Alt	rs121913580(T;T)
Reference	Rs121913580(C;C)
Significance	Pathogenic
Disease	METHYLCOBALAMIN DEFICIENCY
Variation	info
Gene	MTR
CLNDBN	METHYLCOBALAMIN DEFICIENCY, cblG TYPE
Reversed	0
HGVS	NC_000001.10:g.237015878C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015356.27,