rs9606756

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs9606756(A;G)

Make rs9606756(G;G)

Reference

GRCh38 38.1/142

Chromosome

22

Position

30610873

Gene

TCN2

is a	snp
is	mentioned by
dbSNP	rs9606756
dbSNP (classic)	rs9606756
ClinGen	rs9606756
ebi	rs9606756
HLI	rs9606756
Exac	rs9606756
Gnomad	rs9606756
Varsome	rs9606756
LitVar	rs9606756
Map	rs9606756
PheGenI	rs9606756
Biobank	rs9606756
1000 genomes	rs9606756
hgdp	rs9606756
ensembl	rs9606756
geneview	rs9606756
scholar	rs9606756
google	rs9606756
pharmgkb	rs9606756
gwascentral	rs9606756
openSNP	rs9606756
23andMe	rs9606756
SNPshot	rs9606756
SNPdbe	rs9606756
MSV3d	rs9606756
GWAS Ctlg	rs9606756

Max Magnitude

0

?

(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,