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rs74315453

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs74315453(A;A)
Make rs74315453(A;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position42693404
GeneA4GALT
is asnp
is mentioned by
dbSNPrs74315453
ebirs74315453
HLIrs74315453
Exacrs74315453
Varsomers74315453
Maprs74315453
PheGenIrs74315453
hapmaprs74315453
1000 genomesrs74315453
hgdprs74315453
ensemblrs74315453
gopubmedrs74315453
geneviewrs74315453
scholarrs74315453
googlers74315453
pharmgkbrs74315453
gwascentralrs74315453
openSNPrs74315453
23andMers74315453
23andMe allrs74315453
SNP Nexus

SNPshotrs74315453
SNPdbers74315453
MSV3drs74315453
GWAS Ctlgrs74315453
Max Magnitude0
OMIM607922
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315453(A;A)
Alt rs74315453(A;A)
Reference rs74315453(T;T)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43089410A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002811.3,