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rs141179774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141179774(A;A)
Make rs141179774(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position93850180
GeneCRADD
is asnp
is mentioned by
dbSNPrs141179774
dbSNP (old)rs141179774
ClinGenrs141179774
ebirs141179774
HLIrs141179774
Exacrs141179774
Gnomadrs141179774
Varsomers141179774
Maprs141179774
PheGenIrs141179774
Biobankrs141179774
1000 genomesrs141179774
hgdprs141179774
ensemblrs141179774
gopubmedrs141179774
geneviewrs141179774
scholarrs141179774
googlers141179774
pharmgkbrs141179774
gwascentralrs141179774
openSNPrs141179774
23andMers141179774
23andMe allrs141179774
SNPshotrs141179774
SNPdbers141179774
MSV3drs141179774
GWAS Ctlgrs141179774
Max Magnitude0
ClinVar
Risk rs141179774(A;A)
Alt rs141179774(A;A)
Reference Rs141179774(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene CRADD
CLNDBN Mental retardation, autosomal recessive 34
Reversed 0
HGVS NC_000012.11:g.94243956G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412611.1,