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rs1064794298

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome21
Position44889385
GeneITGB2
is asnp
is mentioned by
dbSNPrs1064794298
dbSNP (old)rs1064794298
ClinGenrs1064794298
ebirs1064794298
HLIrs1064794298
Exacrs1064794298
Gnomadrs1064794298
Varsomers1064794298
Maprs1064794298
PheGenIrs1064794298
Biobankrs1064794298
1000 genomesrs1064794298
hgdprs1064794298
ensemblrs1064794298
gopubmedrs1064794298
geneviewrs1064794298
scholarrs1064794298
googlers1064794298
pharmgkbrs1064794298
gwascentralrs1064794298
openSNPrs1064794298
23andMers1064794298
23andMe allrs1064794298
SNPshotrs1064794298
SNPdbers1064794298
MSV3drs1064794298
GWAS Ctlgrs1064794298
Max Magnitude0
ClinVar
Risk rs1064794298(C;C)
Alt rs1064794298(C;C)
Reference Rs1064794298(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ITGB2
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.46309300A>G
CLNSRC
CLNACC RCV000485293.1,