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rs875989848

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989848(-;-)
Make rs875989848(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position26697516
GeneARID1A, LOC101928728
is asnp
is mentioned by
dbSNPrs875989848
ebirs875989848
HLIrs875989848
Exacrs875989848
Varsomers875989848
Maprs875989848
PheGenIrs875989848
hapmaprs875989848
1000 genomesrs875989848
hgdprs875989848
ensemblrs875989848
gopubmedrs875989848
geneviewrs875989848
scholarrs875989848
googlers875989848
pharmgkbrs875989848
gwascentralrs875989848
openSNPrs875989848
23andMers875989848
23andMe allrs875989848
SNP Nexus

SNPshotrs875989848
SNPdbers875989848
MSV3drs875989848
GWAS Ctlgrs875989848
Max Magnitude0
ClinVar
Risk rs875989848(;)
Alt rs875989848(;)
Reference rs875989848(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.27024007delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000211061.1,