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rs1057518614

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057518614(-;-)
Make rs1057518614(-;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position199272470
GeneSATB2
is asnp
is mentioned by
dbSNPrs1057518614
dbSNP (old)rs1057518614
ClinGenrs1057518614
ebirs1057518614
HLIrs1057518614
Exacrs1057518614
Gnomadrs1057518614
Varsomers1057518614
Maprs1057518614
PheGenIrs1057518614
Biobankrs1057518614
1000 genomesrs1057518614
hgdprs1057518614
ensemblrs1057518614
gopubmedrs1057518614
geneviewrs1057518614
scholarrs1057518614
googlers1057518614
pharmgkbrs1057518614
gwascentralrs1057518614
openSNPrs1057518614
23andMers1057518614
23andMe allrs1057518614
SNPshotrs1057518614
SNPdbers1057518614
MSV3drs1057518614
GWAS Ctlgrs1057518614
Max Magnitude0
ClinVar
Risk rs1057518614(-;-)
Alt rs1057518614(-;-)
Reference Rs1057518614(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene SATB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.200137193_200137194delAG
CLNSRC
CLNACC RCV000413155.1,