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rs1064794297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome21
Position44886837
GeneITGB2
is asnp
is mentioned by
dbSNPrs1064794297
dbSNP (old)rs1064794297
ClinGenrs1064794297
ebirs1064794297
HLIrs1064794297
Exacrs1064794297
Gnomadrs1064794297
Varsomers1064794297
LitVarrs1064794297
Maprs1064794297
PheGenIrs1064794297
Biobankrs1064794297
1000 genomesrs1064794297
hgdprs1064794297
ensemblrs1064794297
gopubmedrs1064794297
geneviewrs1064794297
scholarrs1064794297
googlers1064794297
pharmgkbrs1064794297
gwascentralrs1064794297
openSNPrs1064794297
23andMers1064794297
23andMe allrs1064794297
SNPshotrs1064794297
SNPdbers1064794297
MSV3drs1064794297
GWAS Ctlgrs1064794297
Max Magnitude0
ClinVar
Risk rs1064794297(C;C)
Alt rs1064794297(C;C)
Reference Rs1064794297(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ITGB2
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.46306752C>G
CLNSRC
CLNACC RCV000481692.1,