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rs1057519009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519009(-;AA)
Make rs1057519009(AA;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157181120
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057519009
dbSNP (classic)rs1057519009
ClinGenrs1057519009
ebirs1057519009
HLIrs1057519009
Exacrs1057519009
Gnomadrs1057519009
Varsomers1057519009
LitVarrs1057519009
Maprs1057519009
PheGenIrs1057519009
Biobankrs1057519009
1000 genomesrs1057519009
hgdprs1057519009
ensemblrs1057519009
geneviewrs1057519009
scholarrs1057519009
googlers1057519009
pharmgkbrs1057519009
gwascentralrs1057519009
openSNPrs1057519009
23andMers1057519009
23andMe allrs1057519009
SNPshotrs1057519009
SNPdbers1057519009
MSV3drs1057519009
GWAS Ctlgrs1057519009
Max Magnitude0
ClinVar
Risk rs1057519009(AA;AA)
Alt rs1057519009(AA;AA)
Reference Rs1057519009(-;-)
Significance Probable-Pathogenic
Disease Coffin-Siris syndrome
Variation info
Gene ARID1B
CLNDBN Coffin-Siris syndrome
Reversed 0
HGVS NC_000006.11:g.157502253_157502254dupAA
CLNSRC
CLNACC RCV000414768.1,