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rs10418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs10418(C;T)
Make rs10418(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position30626965
GeneTCN2
is asnp
is mentioned by
dbSNPrs10418
dbSNP (classic)rs10418
ClinGenrs10418
ebirs10418
HLIrs10418
Exacrs10418
Gnomadrs10418
Varsomers10418
LitVarrs10418
Maprs10418
PheGenIrs10418
Biobankrs10418
1000 genomesrs10418
hgdprs10418
ensemblrs10418
geneviewrs10418
scholarrs10418
googlers10418
pharmgkbrs10418
gwascentralrs10418
openSNPrs10418
23andMers10418
SNPshotrs10418
SNPdbers10418
MSV3drs10418
GWAS Ctlgrs10418
GMAF0.2571
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23089108] Idiopathic pulmonary fibrosis and polymorphisms of the folate pathway genes


ClinVar
Risk rs10418(T;T)
Alt rs10418(T;T)
Reference Rs10418(C;C)
Significance Non-pathogenic
Disease Transcobalamin II deficiency
Variation info
Gene TCN2
CLNDBN Transcobalamin II deficiency
Reversed 0
HGVS NC_000022.10:g.31022952C>T
CLNSRC
CLNACC RCV000339325.1,