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rs1057520873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520873(G;T)
Make rs1057520873(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position197104888
GeneASPM
is asnp
is mentioned by
dbSNPrs1057520873
dbSNP (old)rs1057520873
ClinGenrs1057520873
ebirs1057520873
HLIrs1057520873
Exacrs1057520873
Gnomadrs1057520873
Varsomers1057520873
LitVarrs1057520873
Maprs1057520873
PheGenIrs1057520873
Biobankrs1057520873
1000 genomesrs1057520873
hgdprs1057520873
ensemblrs1057520873
gopubmedrs1057520873
geneviewrs1057520873
scholarrs1057520873
googlers1057520873
pharmgkbrs1057520873
gwascentralrs1057520873
openSNPrs1057520873
23andMers1057520873
23andMe allrs1057520873
SNPshotrs1057520873
SNPdbers1057520873
MSV3drs1057520873
GWAS Ctlgrs1057520873
Max Magnitude0
ClinVar
Risk rs1057520873(T;T)
Alt rs1057520873(T;T)
Reference Rs1057520873(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197074018C>A
CLNSRC
CLNACC RCV000421420.1,