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rs749462358

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749462358(C;T)
Make rs749462358(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197128656
GeneASPM
is asnp
is mentioned by
dbSNPrs749462358
ebirs749462358
HLIrs749462358
Exacrs749462358
Varsomers749462358
Maprs749462358
PheGenIrs749462358
hapmaprs749462358
1000 genomesrs749462358
hgdprs749462358
ensemblrs749462358
gopubmedrs749462358
geneviewrs749462358
scholarrs749462358
googlers749462358
pharmgkbrs749462358
gwascentralrs749462358
openSNPrs749462358
23andMers749462358
23andMe allrs749462358
SNP Nexus

SNPshotrs749462358
SNPdbers749462358
MSV3drs749462358
GWAS Ctlgrs749462358
Max Magnitude0
ClinVar
Risk rs749462358(T;T)
Alt rs749462358(T;T)
Reference rs749462358(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197097786C>A
CLNSRC
CLNACC RCV000221380.1,