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rs1057518190

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518190(A;A)
Make rs1057518190(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position199328888
GeneSATB2
is asnp
is mentioned by
dbSNPrs1057518190
dbSNP (old)rs1057518190
ClinGenrs1057518190
ebirs1057518190
HLIrs1057518190
Exacrs1057518190
Gnomadrs1057518190
Varsomers1057518190
Maprs1057518190
PheGenIrs1057518190
Biobankrs1057518190
1000 genomesrs1057518190
hgdprs1057518190
ensemblrs1057518190
gopubmedrs1057518190
geneviewrs1057518190
scholarrs1057518190
googlers1057518190
pharmgkbrs1057518190
gwascentralrs1057518190
openSNPrs1057518190
23andMers1057518190
23andMe allrs1057518190
SNPshotrs1057518190
SNPdbers1057518190
MSV3drs1057518190
GWAS Ctlgrs1057518190
Max Magnitude0
ClinVar
Risk rs1057518190(A;A)
Alt rs1057518190(A;A)
Reference Rs1057518190(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SATB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.200193611C>T
CLNSRC
CLNACC RCV000413401.1,