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rs147622433

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147622433(C;T)
Make rs147622433(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197104829
GeneASPM
is asnp
is mentioned by
dbSNPrs147622433
ebirs147622433
HLIrs147622433
Exacrs147622433
Varsomers147622433
Maprs147622433
PheGenIrs147622433
hapmaprs147622433
1000 genomesrs147622433
hgdprs147622433
ensemblrs147622433
gopubmedrs147622433
geneviewrs147622433
scholarrs147622433
googlers147622433
pharmgkbrs147622433
gwascentralrs147622433
openSNPrs147622433
23andMers147622433
23andMe allrs147622433
SNP Nexus

SNPshotrs147622433
SNPdbers147622433
MSV3drs147622433
GWAS Ctlgrs147622433
Max Magnitude0
ClinVar
Risk rs147622433(T;T)
Alt rs147622433(T;T)
Reference rs147622433(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197073959C>T
CLNSRC
CLNACC RCV000221876.1,