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rs797045263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045263(-;-)
Make rs797045263(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position26696797
GeneARID1A
is asnp
is mentioned by
dbSNPrs797045263
dbSNP (old)rs797045263
ClinGenrs797045263
ebirs797045263
HLIrs797045263
Exacrs797045263
Varsomers797045263
Maprs797045263
PheGenIrs797045263
Biobankrs797045263
1000 genomesrs797045263
hgdprs797045263
ensemblrs797045263
gopubmedrs797045263
geneviewrs797045263
scholarrs797045263
googlers797045263
pharmgkbrs797045263
gwascentralrs797045263
openSNPrs797045263
23andMers797045263
23andMe allrs797045263
SNP Nexus

SNPshotrs797045263
SNPdbers797045263
MSV3drs797045263
GWAS Ctlgrs797045263
Max Magnitude0
ClinVar
Risk rs797045263(-;-)
Alt rs797045263(-;-)
Reference Rs797045263(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene LOC101928728 ARID1A
CLNDBN Mental retardation, autosomal dominant 14
Reversed 0
HGVS NC_000001.10:g.27023288delG
CLNSRC
CLNACC RCV000193411.1,