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rs34926152

From SNPedia

Orientationminus
Stabilizedplus
Make rs34926152(A;A)
Make rs34926152(A;C)
Make rs34926152(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position105545332
GeneALCAM
is asnp
is mentioned by
dbSNPrs34926152
ebirs34926152
HLIrs34926152
Exacrs34926152
Varsomers34926152
Maprs34926152
PheGenIrs34926152
hapmaprs34926152
1000 genomesrs34926152
hgdprs34926152
ensemblrs34926152
gopubmedrs34926152
geneviewrs34926152
scholarrs34926152
googlers34926152
pharmgkbrs34926152
gwascentralrs34926152
openSNPrs34926152
23andMers34926152
23andMe allrs34926152
SNP Nexus

SNPshotrs34926152
SNPdbers34926152
MSV3drs34926152
GWAS Ctlgrs34926152
GMAF0.02571
Max Magnitude

[PMID 23507476] ALCAM - Novel multiple sclerosis locus interfering with HLA-DRB1*1501


GET Evidence
ALCAM-M367I
aa_change Met367Ile
aa_change_short M367I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0368098
summary