Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060499771

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499771(C;C)
Make rs1060499771(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position113900063
GeneAP4B1, AP4B1-AS1
is asnp
is mentioned by
dbSNPrs1060499771
dbSNP (old)rs1060499771
ClinGenrs1060499771
ebirs1060499771
HLIrs1060499771
Exacrs1060499771
Gnomadrs1060499771
Varsomers1060499771
Maprs1060499771
PheGenIrs1060499771
Biobankrs1060499771
1000 genomesrs1060499771
hgdprs1060499771
ensemblrs1060499771
gopubmedrs1060499771
geneviewrs1060499771
scholarrs1060499771
googlers1060499771
pharmgkbrs1060499771
gwascentralrs1060499771
openSNPrs1060499771
23andMers1060499771
23andMe allrs1060499771
SNPshotrs1060499771
SNPdbers1060499771
MSV3drs1060499771
GWAS Ctlgrs1060499771
Max Magnitude0
ClinVar
Risk rs1060499771(C;C)
Alt rs1060499771(C;C)
Reference Rs1060499771(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene AP4B1 AP4B1-AS1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000001.10:g.114442685A>G
CLNSRC
CLNACC RCV000454309.1,