rs121913581

Orientation

plus

Stabilized

plus

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

Make rs121913581(G;T)

Make rs121913581(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

236897020

Gene

MTR

is a	snp
is	mentioned by
dbSNP	rs121913581
dbSNP (classic)	rs121913581
ClinGen	rs121913581
ebi	rs121913581
HLI	rs121913581
Exac	rs121913581
Gnomad	rs121913581
Varsome	rs121913581
LitVar	rs121913581
Map	rs121913581
PheGenI	rs121913581
Biobank	rs121913581
1000 genomes	rs121913581
hgdp	rs121913581
ensembl	rs121913581
geneview	rs121913581
scholar	rs121913581
google	rs121913581
pharmgkb	rs121913581
gwascentral	rs121913581
openSNP	rs121913581
23andMe	rs121913581
SNPshot	rs121913581
SNPdbe	rs121913581
MSV3d	rs121913581
GWAS Ctlg	rs121913581

Max Magnitude

0

OMIM	156570
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121913581(T;T)
Alt	rs121913581(T;T)
Reference	Rs121913581(G;G)
Significance	Pathogenic
Disease	METHYLCOBALAMIN DEFICIENCY
Variation	info
Gene	MTR
CLNDBN	METHYLCOBALAMIN DEFICIENCY, cblG TYPE
Reversed	0
HGVS	NC_000001.10:g.237060320G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015357.28,