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rs387906812

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906812(A;A)
Make rs387906812(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position23834152
GeneDERL3, SMARCB1
is asnp
is mentioned by
dbSNPrs387906812
ebirs387906812
HLIrs387906812
Exacrs387906812
Varsomers387906812
Maprs387906812
PheGenIrs387906812
hapmaprs387906812
1000 genomesrs387906812
hgdprs387906812
ensemblrs387906812
gopubmedrs387906812
geneviewrs387906812
scholarrs387906812
googlers387906812
pharmgkbrs387906812
gwascentralrs387906812
openSNPrs387906812
23andMers387906812
23andMe allrs387906812
SNP Nexus

SNPshotrs387906812
SNPdbers387906812
MSV3drs387906812
GWAS Ctlgrs387906812
Max Magnitude0
ClinVar
Risk rs387906812(A;A)
Alt rs387906812(A;A)
Reference rs387906812(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DERL3 SMARCB1
CLNDBN Mental retardation, autosomal dominant 15
Reversed 0
HGVS NC_000022.10:g.24176339G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023124.3,