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rs875989830

From SNPedia

Orientationminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs875989830(-;-)
Make rs875989830(-;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position199348742
GeneSATB2
is asnp
is mentioned by
dbSNPrs875989830
ebirs875989830
HLIrs875989830
Exacrs875989830
Varsomers875989830
Maprs875989830
PheGenIrs875989830
hapmaprs875989830
1000 genomesrs875989830
hgdprs875989830
ensemblrs875989830
gopubmedrs875989830
geneviewrs875989830
scholarrs875989830
googlers875989830
pharmgkbrs875989830
gwascentralrs875989830
openSNPrs875989830
23andMers875989830
23andMe allrs875989830
SNP Nexus

SNPshotrs875989830
SNPdbers875989830
MSV3drs875989830
GWAS Ctlgrs875989830
Max Magnitude0
ClinVar
Risk rs875989830(;)
Alt rs875989830(;)
Reference rs875989830(GT;GT)
Significance Pathogenic
Disease Chromosome 2q32-q33 deletion syndrome
Variation info
Gene SATB2
CLNDBN Chromosome 2q32-q33 deletion syndrome
Reversed 1
HGVS NC_000002.11:g.200213465_200213466delAC
CLNSRC
CLNACC RCV000209866.1,