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rs1057519002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519002(-;-)
Make rs1057519002(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157207498
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057519002
dbSNP (old)rs1057519002
ClinGenrs1057519002
ebirs1057519002
HLIrs1057519002
Exacrs1057519002
Gnomadrs1057519002
Varsomers1057519002
LitVarrs1057519002
Maprs1057519002
PheGenIrs1057519002
Biobankrs1057519002
1000 genomesrs1057519002
hgdprs1057519002
ensemblrs1057519002
gopubmedrs1057519002
geneviewrs1057519002
scholarrs1057519002
googlers1057519002
pharmgkbrs1057519002
gwascentralrs1057519002
openSNPrs1057519002
23andMers1057519002
23andMe allrs1057519002
SNPshotrs1057519002
SNPdbers1057519002
MSV3drs1057519002
GWAS Ctlgrs1057519002
Max Magnitude0
ClinVar
Risk rs1057519002(-;-)
Alt rs1057519002(-;-)
Reference Rs1057519002(T;T)
Significance Probable-Pathogenic
Disease dysmorphy intellectual deficiency
Variation info
Gene ARID1B
CLNDBN dysmorphy intellectual deficiency
Reversed 0
HGVS NC_000006.11:g.157528632delT
CLNSRC
CLNACC RCV000414865.1,