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rs1060499758

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499758(A;A)
Make rs1060499758(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position197094079
GeneASPM
is asnp
is mentioned by
dbSNPrs1060499758
dbSNP (old)rs1060499758
ClinGenrs1060499758
ebirs1060499758
HLIrs1060499758
Exacrs1060499758
Gnomadrs1060499758
Varsomers1060499758
LitVarrs1060499758
Maprs1060499758
PheGenIrs1060499758
Biobankrs1060499758
1000 genomesrs1060499758
hgdprs1060499758
ensemblrs1060499758
gopubmedrs1060499758
geneviewrs1060499758
scholarrs1060499758
googlers1060499758
pharmgkbrs1060499758
gwascentralrs1060499758
openSNPrs1060499758
23andMers1060499758
23andMe allrs1060499758
SNPshotrs1060499758
SNPdbers1060499758
MSV3drs1060499758
GWAS Ctlgrs1060499758
Max Magnitude0
ClinVar
Risk rs1060499758(A;A)
Alt rs1060499758(A;A)
Reference Rs1060499758(G;G)
Significance Probable-Pathogenic
Disease Microcephaly
Variation info
Gene ASPM
CLNDBN Microcephaly
Reversed 1
HGVS NC_000001.10:g.197063209C>T
CLNSRC
CLNACC RCV000454144.1,