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rs1057518268

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057518268(-;-)
Make rs1057518268(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position197142525
GeneASPM
is asnp
is mentioned by
dbSNPrs1057518268
dbSNP (classic)rs1057518268
ClinGenrs1057518268
ebirs1057518268
HLIrs1057518268
Exacrs1057518268
Gnomadrs1057518268
Varsomers1057518268
LitVarrs1057518268
Maprs1057518268
PheGenIrs1057518268
Biobankrs1057518268
1000 genomesrs1057518268
hgdprs1057518268
ensemblrs1057518268
geneviewrs1057518268
scholarrs1057518268
googlers1057518268
pharmgkbrs1057518268
gwascentralrs1057518268
openSNPrs1057518268
23andMers1057518268
23andMe allrs1057518268
SNPshotrs1057518268
SNPdbers1057518268
MSV3drs1057518268
GWAS Ctlgrs1057518268
Max Magnitude0
ClinVar
Risk rs1057518268(-;-)
Alt rs1057518268(-;-)
Reference Rs1057518268(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197111655_197111656delTT
CLNSRC
CLNACC RCV000413189.1,