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rs2853523

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2853523(A;C)
Make rs2853523(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position236898898
GeneMTR
is asnp
is mentioned by
dbSNPrs2853523
dbSNP (classic)rs2853523
ClinGenrs2853523
ebirs2853523
HLIrs2853523
Exacrs2853523
Gnomadrs2853523
Varsomers2853523
LitVarrs2853523
Maprs2853523
PheGenIrs2853523
Biobankrs2853523
1000 genomesrs2853523
hgdprs2853523
ensemblrs2853523
geneviewrs2853523
scholarrs2853523
googlers2853523
pharmgkbrs2853523
gwascentralrs2853523
openSNPrs2853523
23andMers2853523
SNPshotrs2853523
SNPdbers2853523
MSV3drs2853523
GWAS Ctlgrs2853523
GMAF0.2645
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 20871623OA-icon.png] Genetic analysis of six SNPs in candidate genes associated with high cross-race risk of development of thoracic aortic aneurysms and dissections in Chinese Han population

[PMID 18381459OA-icon.png] Genetic variation in the one-carbon transfer pathway and ovarian cancer risk.


ClinVar
Risk rs2853523(C;C)
Alt rs2853523(C;C)
Reference Rs2853523(A;A)
Significance Non-pathogenic
Disease Disorders of Intracellular Cobalamin Metabolism
Variation info
Gene MTR
CLNDBN Disorders of Intracellular Cobalamin Metabolism
Reversed 0
HGVS NC_000001.10:g.237062198A>C
CLNSRC
CLNACC RCV000360926.1,