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rs750664956

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs750664956(-;-)
Make rs750664956(-;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position197103067
GeneASPM
is asnp
is mentioned by
dbSNPrs750664956
ebirs750664956
HLIrs750664956
Exacrs750664956
Varsomers750664956
Maprs750664956
PheGenIrs750664956
hapmaprs750664956
1000 genomesrs750664956
hgdprs750664956
ensemblrs750664956
gopubmedrs750664956
geneviewrs750664956
scholarrs750664956
googlers750664956
pharmgkbrs750664956
gwascentralrs750664956
openSNPrs750664956
23andMers750664956
23andMe allrs750664956
SNP Nexus

SNPshotrs750664956
SNPdbers750664956
MSV3drs750664956
GWAS Ctlgrs750664956
Max Magnitude0
ClinVar
Risk rs750664956(;)
Alt rs750664956(;)
Reference rs750664956(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.197072197_197072198delTC
CLNSRC
CLNACC RCV000217980.1,