Have questions? Visit https://www.reddit.com/r/SNPedia

rs876661154

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661154(-;-)
Make rs876661154(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197100652
GeneASPM
is asnp
is mentioned by
dbSNPrs876661154
ebirs876661154
HLIrs876661154
Exacrs876661154
Varsomers876661154
Maprs876661154
PheGenIrs876661154
hapmaprs876661154
1000 genomesrs876661154
hgdprs876661154
ensemblrs876661154
gopubmedrs876661154
geneviewrs876661154
scholarrs876661154
googlers876661154
pharmgkbrs876661154
gwascentralrs876661154
openSNPrs876661154
23andMers876661154
23andMe allrs876661154
SNP Nexus

SNPshotrs876661154
SNPdbers876661154
MSV3drs876661154
GWAS Ctlgrs876661154
Max Magnitude0
ClinVar
Risk rs876661154(;)
Alt rs876661154(;)
Reference rs876661154(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197069782delG
CLNSRC
CLNACC RCV000222135.1,