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rs387906861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906861(C;C)
Make rs387906861(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position93850053
GeneCRADD
is asnp
is mentioned by
dbSNPrs387906861
ebirs387906861
HLIrs387906861
Exacrs387906861
Varsomers387906861
Maprs387906861
PheGenIrs387906861
hapmaprs387906861
1000 genomesrs387906861
hgdprs387906861
ensemblrs387906861
gopubmedrs387906861
geneviewrs387906861
scholarrs387906861
googlers387906861
pharmgkbrs387906861
gwascentralrs387906861
openSNPrs387906861
23andMers387906861
23andMe allrs387906861
SNP Nexus

SNPshotrs387906861
SNPdbers387906861
MSV3drs387906861
GWAS Ctlgrs387906861
Max Magnitude0
ClinVar
Risk rs387906861(C;C)
Alt rs387906861(C;C)
Reference rs387906861(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CRADD
CLNDBN Mental retardation, autosomal recessive 34
Reversed 0
HGVS NC_000012.11:g.94243829G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023305.2,