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rs372108744

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372108744(C;T)
Make rs372108744(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position241801858
GeneGAL3ST2
is asnp
is mentioned by
dbSNPrs372108744
ebirs372108744
HLIrs372108744
Exacrs372108744
Varsomers372108744
Maprs372108744
PheGenIrs372108744
hapmaprs372108744
1000 genomesrs372108744
hgdprs372108744
ensemblrs372108744
gopubmedrs372108744
geneviewrs372108744
scholarrs372108744
googlers372108744
pharmgkbrs372108744
gwascentralrs372108744
openSNPrs372108744
23andMers372108744
23andMe allrs372108744
SNP Nexus

SNPshotrs372108744
SNPdbers372108744
MSV3drs372108744
GWAS Ctlgrs372108744
Max Magnitude0
ClinVar
Risk rs372108744(T;T)
Alt rs372108744(T;T)
Reference rs372108744(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GAL3ST2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.242741273C>T
CLNSRC
CLNACC RCV000171122.1,