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rs876660960

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660960(-;-)
Make rs876660960(-;A)
Make rs876660960(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197101207
GeneASPM
is asnp
is mentioned by
dbSNPrs876660960
ebirs876660960
HLIrs876660960
Exacrs876660960
Varsomers876660960
Maprs876660960
PheGenIrs876660960
hapmaprs876660960
1000 genomesrs876660960
hgdprs876660960
ensemblrs876660960
gopubmedrs876660960
geneviewrs876660960
scholarrs876660960
googlers876660960
pharmgkbrs876660960
gwascentralrs876660960
openSNPrs876660960
23andMers876660960
23andMe allrs876660960
SNP Nexus

SNPshotrs876660960
SNPdbers876660960
MSV3drs876660960
GWAS Ctlgrs876660960
Max Magnitude0
ClinVar
Risk rs876660960(A;A)
Alt rs876660960(A;A)
Reference rs876660960(;)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197070338dupT
CLNSRC
CLNACC RCV000217588.1,