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rs876660961

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660961(-;-)
Make rs876660961(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197092014
GeneASPM
is asnp
is mentioned by
dbSNPrs876660961
ebirs876660961
HLIrs876660961
Exacrs876660961
Varsomers876660961
Maprs876660961
PheGenIrs876660961
hapmaprs876660961
1000 genomesrs876660961
hgdprs876660961
ensemblrs876660961
gopubmedrs876660961
geneviewrs876660961
scholarrs876660961
googlers876660961
pharmgkbrs876660961
gwascentralrs876660961
openSNPrs876660961
23andMers876660961
23andMe allrs876660961
SNP Nexus

SNPshotrs876660961
SNPdbers876660961
MSV3drs876660961
GWAS Ctlgrs876660961
Max Magnitude0
ClinVar
Risk rs876660961(;)
Alt rs876660961(;)
Reference rs876660961(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197061144delC
CLNSRC
CLNACC RCV000218838.1,