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rs1800028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1800028(C;T)
Make rs1800028(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position48703560
GeneFUT2, LOC105447645
is asnp
is mentioned by
dbSNPrs1800028
dbSNP (old)rs1800028
ClinGenrs1800028
ebirs1800028
HLIrs1800028
Exacrs1800028
Gnomadrs1800028
Varsomers1800028
LitVarrs1800028
Maprs1800028
PheGenIrs1800028
Biobankrs1800028
1000 genomesrs1800028
hgdprs1800028
ensemblrs1800028
gopubmedrs1800028
geneviewrs1800028
scholarrs1800028
googlers1800028
pharmgkbrs1800028
gwascentralrs1800028
openSNPrs1800028
23andMers1800028
23andMe allrs1800028
SNPshotrs1800028
SNPdbers1800028
MSV3drs1800028
GWAS Ctlgrs1800028
Max Magnitude0
ClinVar
Risk rs1800028(T;T)
Alt rs1800028(T;T)
Reference Rs1800028(C;C)
Significance Pathogenic
Disease Vitamin b12 plasma level quantitative trait locus 1
Variation info
Gene FUT2 LOC105447645
CLNDBN Vitamin b12 plasma level quantitative trait locus 1
Reversed 0
HGVS NC_000019.9:g.49206817C>T
CLNSRC
CLNACC RCV000490450.1,