Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044445(-;A)
Make rs797044445(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position236894532
GeneMTR
is asnp
is mentioned by
dbSNPrs797044445
ClinGenrs797044445
ebirs797044445
HLIrs797044445
Exacrs797044445
Varsomers797044445
Maprs797044445
PheGenIrs797044445
hapmaprs797044445
1000 genomesrs797044445
hgdprs797044445
ensemblrs797044445
gopubmedrs797044445
geneviewrs797044445
scholarrs797044445
googlers797044445
pharmgkbrs797044445
gwascentralrs797044445
openSNPrs797044445
23andMers797044445
23andMe allrs797044445
SNP Nexus

SNPshotrs797044445
SNPdbers797044445
MSV3drs797044445
GWAS Ctlgrs797044445
Max Magnitude0
ClinVar
Risk rs797044445(A;A)
Alt rs797044445(A;A)
Reference Rs797044445(-;-)
Significance Pathogenic
Disease METHYLCOBALAMIN DEFICIENCY
Variation info
Gene MTR
CLNDBN METHYLCOBALAMIN DEFICIENCY, cblG TYPE
Reversed 0
HGVS NC_000001.10:g.237057832dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000015354.27,