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rs876661036

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661036(G;G)
Make rs876661036(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197101127
GeneASPM
is asnp
is mentioned by
dbSNPrs876661036
ebirs876661036
HLIrs876661036
Exacrs876661036
Varsomers876661036
Maprs876661036
PheGenIrs876661036
hapmaprs876661036
1000 genomesrs876661036
hgdprs876661036
ensemblrs876661036
gopubmedrs876661036
geneviewrs876661036
scholarrs876661036
googlers876661036
pharmgkbrs876661036
gwascentralrs876661036
openSNPrs876661036
23andMers876661036
23andMe allrs876661036
SNP Nexus

SNPshotrs876661036
SNPdbers876661036
MSV3drs876661036
GWAS Ctlgrs876661036
Max Magnitude0
ClinVar
Risk rs876661036(G;G)
Alt rs876661036(G;G)
Reference rs876661036(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197070257A>C
CLNSRC
CLNACC RCV000213452.1,