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rs753406334

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753406334(C;C)
Make rs753406334(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197104519
GeneASPM
is asnp
is mentioned by
dbSNPrs753406334
ebirs753406334
HLIrs753406334
Exacrs753406334
Varsomers753406334
Maprs753406334
PheGenIrs753406334
hapmaprs753406334
1000 genomesrs753406334
hgdprs753406334
ensemblrs753406334
gopubmedrs753406334
geneviewrs753406334
scholarrs753406334
googlers753406334
pharmgkbrs753406334
gwascentralrs753406334
openSNPrs753406334
23andMers753406334
23andMe allrs753406334
SNP Nexus

SNPshotrs753406334
SNPdbers753406334
MSV3drs753406334
GWAS Ctlgrs753406334
Max Magnitude0
ClinVar
Risk rs753406334(A,C;A,C)
Alt rs753406334(A,C;A,C)
Reference rs753406334(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197073649G>A
CLNSRC
CLNACC RCV000220667.1,