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rs875989849

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989849(G;T)
Make rs875989849(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position26772951
GeneARID1A
is asnp
is mentioned by
dbSNPrs875989849
ebirs875989849
HLIrs875989849
Exacrs875989849
Varsomers875989849
Maprs875989849
PheGenIrs875989849
hapmaprs875989849
1000 genomesrs875989849
hgdprs875989849
ensemblrs875989849
gopubmedrs875989849
geneviewrs875989849
scholarrs875989849
googlers875989849
pharmgkbrs875989849
gwascentralrs875989849
openSNPrs875989849
23andMers875989849
23andMe allrs875989849
SNP Nexus

SNPshotrs875989849
SNPdbers875989849
MSV3drs875989849
GWAS Ctlgrs875989849
Max Magnitude0
ClinVar
Risk rs875989849(T;T)
Alt rs875989849(T;T)
Reference rs875989849(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene ARID1A
CLNDBN Mental retardation, autosomal dominant 14
Reversed 0
HGVS NC_000001.10:g.27099442G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000211078.1,