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rs1057518269

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518269(A;A)
Make rs1057518269(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position197133360
GeneASPM
is asnp
is mentioned by
dbSNPrs1057518269
dbSNP (old)rs1057518269
ClinGenrs1057518269
ebirs1057518269
HLIrs1057518269
Exacrs1057518269
Gnomadrs1057518269
Varsomers1057518269
Maprs1057518269
PheGenIrs1057518269
Biobankrs1057518269
1000 genomesrs1057518269
hgdprs1057518269
ensemblrs1057518269
gopubmedrs1057518269
geneviewrs1057518269
scholarrs1057518269
googlers1057518269
pharmgkbrs1057518269
gwascentralrs1057518269
openSNPrs1057518269
23andMers1057518269
23andMe allrs1057518269
SNPshotrs1057518269
SNPdbers1057518269
MSV3drs1057518269
GWAS Ctlgrs1057518269
Max Magnitude0
ClinVar
Risk rs1057518269(A;A)
Alt rs1057518269(A;A)
Reference Rs1057518269(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197102490C>T
CLNSRC
CLNACC RCV000413809.1,