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rs9606756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9606756(A;G)
Make rs9606756(G;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position30610873
GeneTCN2
is asnp
is mentioned by
dbSNPrs9606756
dbSNP (old)rs9606756
ClinGenrs9606756
ebirs9606756
HLIrs9606756
Exacrs9606756
Gnomadrs9606756
Varsomers9606756
Maprs9606756
PheGenIrs9606756
Biobankrs9606756
1000 genomesrs9606756
hgdprs9606756
ensemblrs9606756
gopubmedrs9606756
geneviewrs9606756
scholarrs9606756
googlers9606756
pharmgkbrs9606756
gwascentralrs9606756
openSNPrs9606756
23andMers9606756
23andMe allrs9606756
SNP Nexus

SNPshotrs9606756
SNPdbers9606756
MSV3drs9606756
GWAS Ctlgrs9606756
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 25681243] Single nucleotide polymorphisms related to vitamin B12 serum levels in autoimmune gastritis patients with or without pernicious anaemia


ClinVar
Risk rs9606756(G;G)
Alt rs9606756(G;G)
Reference Rs9606756(A;A)
Significance Probable-non-pathogenic
Disease Transcobalamin II deficiency
Variation info
Gene TCN2
CLNDBN Transcobalamin II deficiency
Reversed 0
HGVS NC_000022.10:g.31006860A>G
CLNSRC
CLNACC RCV000398328.1,