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rs797044874

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044874(C;T)
Make rs797044874(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position199349027
GeneSATB2
is asnp
is mentioned by
dbSNPrs797044874
ebirs797044874
HLIrs797044874
Exacrs797044874
Varsomers797044874
Maprs797044874
PheGenIrs797044874
hapmaprs797044874
1000 genomesrs797044874
hgdprs797044874
ensemblrs797044874
gopubmedrs797044874
geneviewrs797044874
scholarrs797044874
googlers797044874
pharmgkbrs797044874
gwascentralrs797044874
openSNPrs797044874
23andMers797044874
23andMe allrs797044874
SNP Nexus

SNPshotrs797044874
SNPdbers797044874
MSV3drs797044874
GWAS Ctlgrs797044874
Max Magnitude0
ClinVar
Risk rs797044874(T;T)
Alt rs797044874(T;T)
Reference rs797044874(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SATB2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000002.11:g.200213750G>A
CLNSRC
CLNACC RCV000190685.1,