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rs1057518556

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518556(A;A)
Make rs1057518556(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position197142578
GeneASPM
is asnp
is mentioned by
dbSNPrs1057518556
dbSNP (old)rs1057518556
ClinGenrs1057518556
ebirs1057518556
HLIrs1057518556
Exacrs1057518556
Gnomadrs1057518556
Varsomers1057518556
Maprs1057518556
PheGenIrs1057518556
Biobankrs1057518556
1000 genomesrs1057518556
hgdprs1057518556
ensemblrs1057518556
gopubmedrs1057518556
geneviewrs1057518556
scholarrs1057518556
googlers1057518556
pharmgkbrs1057518556
gwascentralrs1057518556
openSNPrs1057518556
23andMers1057518556
23andMe allrs1057518556
SNPshotrs1057518556
SNPdbers1057518556
MSV3drs1057518556
GWAS Ctlgrs1057518556
Max Magnitude0
ClinVar
Risk rs1057518556(A;A)
Alt rs1057518556(A;A)
Reference Rs1057518556(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197111708A>T
CLNSRC
CLNACC RCV000413862.1,