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rs869312697

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312697(C;T)
Make rs869312697(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position157207241
GeneARID1B
is asnp
is mentioned by
dbSNPrs869312697
ebirs869312697
HLIrs869312697
Exacrs869312697
Varsomers869312697
Maprs869312697
PheGenIrs869312697
hapmaprs869312697
1000 genomesrs869312697
hgdprs869312697
ensemblrs869312697
gopubmedrs869312697
geneviewrs869312697
scholarrs869312697
googlers869312697
pharmgkbrs869312697
gwascentralrs869312697
openSNPrs869312697
23andMers869312697
23andMe allrs869312697
SNP Nexus

SNPshotrs869312697
SNPdbers869312697
MSV3drs869312697
GWAS Ctlgrs869312697
Max Magnitude0
ClinVar
Risk rs869312697(T;T)
Alt rs869312697(T;T)
Reference rs869312697(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157528375C>T
CLNSRC
CLNACC RCV000209939.1,