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rs1064794638

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position199381775
GeneSATB2
is asnp
is mentioned by
dbSNPrs1064794638
dbSNP (old)rs1064794638
ClinGenrs1064794638
ebirs1064794638
HLIrs1064794638
Exacrs1064794638
Gnomadrs1064794638
Varsomers1064794638
Maprs1064794638
PheGenIrs1064794638
Biobankrs1064794638
1000 genomesrs1064794638
hgdprs1064794638
ensemblrs1064794638
gopubmedrs1064794638
geneviewrs1064794638
scholarrs1064794638
googlers1064794638
pharmgkbrs1064794638
gwascentralrs1064794638
openSNPrs1064794638
23andMers1064794638
23andMe allrs1064794638
SNPshotrs1064794638
SNPdbers1064794638
MSV3drs1064794638
GWAS Ctlgrs1064794638
Max Magnitude0
ClinVar
Risk rs1064794638(A;A)
Alt rs1064794638(A;A)
Reference Rs1064794638(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SATB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.200246498A>T
CLNSRC
CLNACC RCV000485195.1,