Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060499762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499762(A;T)
Make rs1060499762(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position112647384
GeneLARP7, LOC109864269, MIR367
is asnp
is mentioned by
dbSNPrs1060499762
dbSNP (old)rs1060499762
ClinGenrs1060499762
ebirs1060499762
HLIrs1060499762
Exacrs1060499762
Gnomadrs1060499762
Varsomers1060499762
Maprs1060499762
PheGenIrs1060499762
Biobankrs1060499762
1000 genomesrs1060499762
hgdprs1060499762
ensemblrs1060499762
gopubmedrs1060499762
geneviewrs1060499762
scholarrs1060499762
googlers1060499762
pharmgkbrs1060499762
gwascentralrs1060499762
openSNPrs1060499762
23andMers1060499762
23andMe allrs1060499762
SNPshotrs1060499762
SNPdbers1060499762
MSV3drs1060499762
GWAS Ctlgrs1060499762
Max Magnitude0
ClinVar
Risk rs1060499762(T;T)
Alt rs1060499762(T;T)
Reference Rs1060499762(A;A)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene LOC109864269 LARP7 MIR367
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000004.11:g.113568540A>T
CLNSRC
CLNACC RCV000454270.1,