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rs1057518691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518691(C;C)
Make rs1057518691(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157189781
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057518691
dbSNP (old)rs1057518691
ClinGenrs1057518691
ebirs1057518691
HLIrs1057518691
Exacrs1057518691
Gnomadrs1057518691
Varsomers1057518691
LitVarrs1057518691
Maprs1057518691
PheGenIrs1057518691
Biobankrs1057518691
1000 genomesrs1057518691
hgdprs1057518691
ensemblrs1057518691
gopubmedrs1057518691
geneviewrs1057518691
scholarrs1057518691
googlers1057518691
pharmgkbrs1057518691
gwascentralrs1057518691
openSNPrs1057518691
23andMers1057518691
23andMe allrs1057518691
SNPshotrs1057518691
SNPdbers1057518691
MSV3drs1057518691
GWAS Ctlgrs1057518691
Max Magnitude0
ClinVar
Risk rs1057518691(C;C)
Alt rs1057518691(C;C)
Reference Rs1057518691(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157510915G>C
CLNSRC
CLNACC RCV000415272.1,