Rs137853061

Orientation

plus

is a	snp
is	mentioned by
dbSNP	rs137853061
PheGenI	rs137853061
nextbio	rs137853061
hapmap	rs137853061
1000 genomes	rs137853061
hgdp	rs137853061
ensembl	rs137853061
gopubmed	rs137853061
geneview	rs137853061
scholar	rs137853061
google	rs137853061
pharmgkb	rs137853061
gwascentral	rs137853061
openSNP	rs137853061
23andMe	rs137853061
23andMe all	rs137853061
SNP Nexus
SNPshot	rs137853061
SNPdbe	rs137853061
MSV3d	rs137853061

Gene

MTRR

Chromosome

5

Orientation

plus

Position

7892928

Reference

GRCh37.p5 37.3/135

Max Magnitude

0

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

Make rs137853061(A;A)

Make rs137853061(A;G)

OMIM	602568
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137853061(A;A)
Normal	rs137853061(G;G)
Significance	5
Disease	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN M
ClinVar	info
Gene	MTRR
CLNDBN	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN M
Reversed	0
CLNHGVS	NC_000005.9:g.7892928G>A
CLNSRC	OMIM Allelic Variant