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rs753424199

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs753424199(-;-)
Make rs753424199(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197143097
GeneASPM
is asnp
is mentioned by
dbSNPrs753424199
ebirs753424199
HLIrs753424199
Exacrs753424199
Varsomers753424199
Maprs753424199
PheGenIrs753424199
hapmaprs753424199
1000 genomesrs753424199
hgdprs753424199
ensemblrs753424199
gopubmedrs753424199
geneviewrs753424199
scholarrs753424199
googlers753424199
pharmgkbrs753424199
gwascentralrs753424199
openSNPrs753424199
23andMers753424199
23andMe allrs753424199
SNP Nexus

SNPshotrs753424199
SNPdbers753424199
MSV3drs753424199
GWAS Ctlgrs753424199
Max Magnitude0
ClinVar
Risk rs753424199(;)
Alt rs753424199(;)
Reference rs753424199(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197112227_197112228delCT
CLNSRC
CLNACC RCV000219412.1,