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rs879255529

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255529(-;-)
Make rs879255529(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position45848963
GeneARID2, LOC105369745
is asnp
is mentioned by
dbSNPrs879255529
ClinGenrs879255529
ebirs879255529
HLIrs879255529
Exacrs879255529
Varsomers879255529
Maprs879255529
PheGenIrs879255529
hapmaprs879255529
1000 genomesrs879255529
hgdprs879255529
ensemblrs879255529
gopubmedrs879255529
geneviewrs879255529
scholarrs879255529
googlers879255529
pharmgkbrs879255529
gwascentralrs879255529
openSNPrs879255529
23andMers879255529
23andMe allrs879255529
SNP Nexus

SNPshotrs879255529
SNPdbers879255529
MSV3drs879255529
GWAS Ctlgrs879255529
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs879255529(T;T)
Significance Pathogenic
Disease Abnormal facial shape Intellectual disability (moderate)
Variation info
Gene ARID2
CLNDBN Abnormal facial shape Intellectual disability (moderate)
Reversed 0
HGVS NC_000012.11:g.46242746delT
CLNSRC
CLNACC RCV000239407.1,