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rs1060499668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499668(C;T)
Make rs1060499668(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position156829419
GeneARID1B
is asnp
is mentioned by
dbSNPrs1060499668
dbSNP (old)rs1060499668
ClinGenrs1060499668
ebirs1060499668
HLIrs1060499668
Exacrs1060499668
Gnomadrs1060499668
Varsomers1060499668
Maprs1060499668
PheGenIrs1060499668
Biobankrs1060499668
1000 genomesrs1060499668
hgdprs1060499668
ensemblrs1060499668
gopubmedrs1060499668
geneviewrs1060499668
scholarrs1060499668
googlers1060499668
pharmgkbrs1060499668
gwascentralrs1060499668
openSNPrs1060499668
23andMers1060499668
23andMe allrs1060499668
SNPshotrs1060499668
SNPdbers1060499668
MSV3drs1060499668
GWAS Ctlgrs1060499668
Max Magnitude0
ClinVar
Risk rs1060499668(T;T)
Alt rs1060499668(T;T)
Reference Rs1060499668(C;C)
Significance Pathogenic
Disease Nicolaides-Baraitser syndrome
Variation info
Gene ARID1B
CLNDBN Nicolaides-Baraitser syndrome
Reversed 0
HGVS NC_000006.11:g.157150553C>T
CLNSRC
CLNACC RCV000449505.1,