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rs387906279

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Make rs387906279(-;-)
Make rs387906279(-;CTT)
Make rs387906279(CTT;CTT)
ReferenceGRCh38 38.1/141
Chromosome22
Position42693710
GeneA4GALT
is asnp
is mentioned by
dbSNPrs387906279
ebirs387906279
HLIrs387906279
Exacrs387906279
Varsomers387906279
Maprs387906279
PheGenIrs387906279
hapmaprs387906279
1000 genomesrs387906279
hgdprs387906279
ensemblrs387906279
gopubmedrs387906279
geneviewrs387906279
scholarrs387906279
googlers387906279
pharmgkbrs387906279
gwascentralrs387906279
openSNPrs387906279
23andMers387906279
23andMe allrs387906279
SNP Nexus

SNPshotrs387906279
SNPdbers387906279
MSV3drs387906279
GWAS Ctlgrs387906279
Max Magnitude0
ClinVar
Risk rs387906279(;)
Alt rs387906279(;)
Reference rs387906279(TTC;TTC)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43089716_43089718delAAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000002815.3,