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rs797045281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045281(-;-)
Make rs797045281(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157206294
GeneARID1B
is asnp
is mentioned by
dbSNPrs797045281
dbSNP (classic)rs797045281
ClinGenrs797045281
ebirs797045281
HLIrs797045281
Exacrs797045281
Gnomadrs797045281
Varsomers797045281
LitVarrs797045281
Maprs797045281
PheGenIrs797045281
Biobankrs797045281
1000 genomesrs797045281
hgdprs797045281
ensemblrs797045281
geneviewrs797045281
scholarrs797045281
googlers797045281
pharmgkbrs797045281
gwascentralrs797045281
openSNPrs797045281
23andMers797045281
SNPshotrs797045281
SNPdbers797045281
MSV3drs797045281
GWAS Ctlgrs797045281
Max Magnitude0
ClinVar
Risk rs797045281(-;-)
Alt rs797045281(-;-)
Reference Rs797045281(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157527428delA
CLNSRC
CLNACC RCV000194488.1,