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rs1057521083

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521083(C;T)
Make rs1057521083(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position199348709
GeneSATB2
is asnp
is mentioned by
dbSNPrs1057521083
dbSNP (old)rs1057521083
ClinGenrs1057521083
ebirs1057521083
HLIrs1057521083
Exacrs1057521083
Gnomadrs1057521083
Varsomers1057521083
Maprs1057521083
PheGenIrs1057521083
Biobankrs1057521083
1000 genomesrs1057521083
hgdprs1057521083
ensemblrs1057521083
gopubmedrs1057521083
geneviewrs1057521083
scholarrs1057521083
googlers1057521083
pharmgkbrs1057521083
gwascentralrs1057521083
openSNPrs1057521083
23andMers1057521083
23andMe allrs1057521083
SNPshotrs1057521083
SNPdbers1057521083
MSV3drs1057521083
GWAS Ctlgrs1057521083
Max Magnitude0
ClinVar
Risk rs1057521083(T;T)
Alt rs1057521083(T;T)
Reference Rs1057521083(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SATB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.200213432G>A
CLNSRC
CLNACC RCV000430827.1,