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rs876660959

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660959(-;-)
Make rs876660959(-;A)
Make rs876660959(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197101954
GeneASPM
is asnp
is mentioned by
dbSNPrs876660959
ebirs876660959
HLIrs876660959
Exacrs876660959
Varsomers876660959
Maprs876660959
PheGenIrs876660959
hapmaprs876660959
1000 genomesrs876660959
hgdprs876660959
ensemblrs876660959
gopubmedrs876660959
geneviewrs876660959
scholarrs876660959
googlers876660959
pharmgkbrs876660959
gwascentralrs876660959
openSNPrs876660959
23andMers876660959
23andMe allrs876660959
SNP Nexus

SNPshotrs876660959
SNPdbers876660959
MSV3drs876660959
GWAS Ctlgrs876660959
Max Magnitude0
ClinVar
Risk rs876660959(A;A)
Alt rs876660959(A;A)
Reference rs876660959(;)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197071085dupT
CLNSRC
CLNACC RCV000217938.1,