Rs137853061

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853061(A;A)
Make rs137853061(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position7892815
GeneMTRR
is asnp
is mentioned by
dbSNPrs137853061
Exacrs137853061
PheGenIrs137853061
nextbiors137853061
hapmaprs137853061
1000 genomesrs137853061
hgdprs137853061
ensemblrs137853061
gopubmedrs137853061
geneviewrs137853061
scholarrs137853061
googlers137853061
pharmgkbrs137853061
gwascentralrs137853061
openSNPrs137853061
23andMers137853061
23andMe allrs137853061
SNP Nexus

SNPshotrs137853061
SNPdbers137853061
MSV3drs137853061
OMIM602568
Desc
Variant0004
Relatedalso
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
Variation info
Gene MTRR
CLNDBN Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type
Reversed 0
HGVS NC_000005.9:g.7892928G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007446.2,