rs137853061

Orientation

plus

Stabilized

plus

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

Make rs137853061(A;A)

Make rs137853061(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

7892815

Gene

MTRR

is a	snp
is	mentioned by
dbSNP	rs137853061
dbSNP (classic)	rs137853061
ClinGen	rs137853061
ebi	rs137853061
HLI	rs137853061
Exac	rs137853061
Gnomad	rs137853061
Varsome	rs137853061
LitVar	rs137853061
Map	rs137853061
PheGenI	rs137853061
Biobank	rs137853061
1000 genomes	rs137853061
hgdp	rs137853061
ensembl	rs137853061
geneview	rs137853061
scholar	rs137853061
google	rs137853061
pharmgkb	rs137853061
gwascentral	rs137853061
openSNP	rs137853061
23andMe	rs137853061
SNPshot	rs137853061
SNPdbe	rs137853061
MSV3d	rs137853061
GWAS Ctlg	rs137853061

Max Magnitude

0

OMIM	602568
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137853061(A;A)
Alt	rs137853061(A;A)
Reference	Rs137853061(G;G)
Significance	Pathogenic
Disease	Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism Inborn genetic diseases
Variation	info
Gene	MTRR
CLNDBN	Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Inborn genetic diseases
Reversed	0
HGVS	NC_000005.9:g.7892928G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007446.3, RCV000210727.1,