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rs199422137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs199422137(-;-)
Make rs199422137(-;AG)
ReferenceGRCh38 38.1/141
Chromosome1
Position197143099
GeneASPM
is asnp
is mentioned by
dbSNPrs199422137
ebirs199422137
HLIrs199422137
Exacrs199422137
Varsomers199422137
Maprs199422137
PheGenIrs199422137
hapmaprs199422137
1000 genomesrs199422137
hgdprs199422137
ensemblrs199422137
gopubmedrs199422137
geneviewrs199422137
scholarrs199422137
googlers199422137
pharmgkbrs199422137
gwascentralrs199422137
openSNPrs199422137
23andMers199422137
23andMe allrs199422137
SNP Nexus

SNPshotrs199422137
SNPdbers199422137
MSV3drs199422137
GWAS Ctlgrs199422137
Max Magnitude0
ClinVar
Risk rs199422137(;)
Alt rs199422137(;)
Reference rs199422137(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197112227_197112228delCT
CLNSRC ClinVar GeneReviews
CLNACC RCV000219412.1,