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rs74315454

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315454(A;A)
Make rs74315454(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position42693169
GeneA4GALT
is asnp
is mentioned by
dbSNPrs74315454
ebirs74315454
HLIrs74315454
Exacrs74315454
Varsomers74315454
Maprs74315454
PheGenIrs74315454
hapmaprs74315454
1000 genomesrs74315454
hgdprs74315454
ensemblrs74315454
gopubmedrs74315454
geneviewrs74315454
scholarrs74315454
googlers74315454
pharmgkbrs74315454
gwascentralrs74315454
openSNPrs74315454
23andMers74315454
23andMe allrs74315454
SNP Nexus

SNPshotrs74315454
SNPdbers74315454
MSV3drs74315454
GWAS Ctlgrs74315454
Max Magnitude0
OMIM607922
Desc
Variant0003
Relatedalso
ClinVar
Risk rs74315454(A,C;A,C)
Alt rs74315454(A,C;A,C)
Reference rs74315454(G;G)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43089175C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002813.3,