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rs1060499748

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499748(A;A)
Make rs1060499748(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position23988262
GeneKLHL15
is asnp
is mentioned by
dbSNPrs1060499748
dbSNP (old)rs1060499748
ClinGenrs1060499748
ebirs1060499748
HLIrs1060499748
Exacrs1060499748
Gnomadrs1060499748
Varsomers1060499748
Maprs1060499748
PheGenIrs1060499748
Biobankrs1060499748
1000 genomesrs1060499748
hgdprs1060499748
ensemblrs1060499748
gopubmedrs1060499748
geneviewrs1060499748
scholarrs1060499748
googlers1060499748
pharmgkbrs1060499748
gwascentralrs1060499748
openSNPrs1060499748
23andMers1060499748
23andMe allrs1060499748
SNPshotrs1060499748
SNPdbers1060499748
MSV3drs1060499748
GWAS Ctlgrs1060499748
Max Magnitude0
ClinVar
Risk rs1060499748(A;A)
Alt rs1060499748(A;A)
Reference Rs1060499748(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene KLHL15
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000023.10:g.24006379C>T
CLNSRC
CLNACC RCV000454336.1,