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rs1057518496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518496(C;T)
Make rs1057518496(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position199349006
GeneSATB2
is asnp
is mentioned by
dbSNPrs1057518496
dbSNP (old)rs1057518496
ClinGenrs1057518496
ebirs1057518496
HLIrs1057518496
Exacrs1057518496
Gnomadrs1057518496
Varsomers1057518496
Maprs1057518496
PheGenIrs1057518496
Biobankrs1057518496
1000 genomesrs1057518496
hgdprs1057518496
ensemblrs1057518496
gopubmedrs1057518496
geneviewrs1057518496
scholarrs1057518496
googlers1057518496
pharmgkbrs1057518496
gwascentralrs1057518496
openSNPrs1057518496
23andMers1057518496
23andMe allrs1057518496
SNPshotrs1057518496
SNPdbers1057518496
MSV3drs1057518496
GWAS Ctlgrs1057518496
Max Magnitude0
ClinVar
Risk rs1057518496(T;T)
Alt rs1057518496(T;T)
Reference Rs1057518496(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SATB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.200213729G>A
CLNSRC
CLNACC RCV000413829.1,