Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205609

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205609(-;-)
Make rs786205609(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position197104187
GeneASPM
is asnp
is mentioned by
dbSNPrs786205609
ebirs786205609
HLIrs786205609
Exacrs786205609
Varsomers786205609
Maprs786205609
PheGenIrs786205609
hapmaprs786205609
1000 genomesrs786205609
hgdprs786205609
ensemblrs786205609
gopubmedrs786205609
geneviewrs786205609
scholarrs786205609
googlers786205609
pharmgkbrs786205609
gwascentralrs786205609
openSNPrs786205609
23andMers786205609
23andMe allrs786205609
SNP Nexus

SNPshotrs786205609
SNPdbers786205609
MSV3drs786205609
GWAS Ctlgrs786205609
Max Magnitude0
ClinVar
Risk rs786205609(;)
Alt rs786205609(;)
Reference rs786205609(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASPM
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.197073317delA
CLNSRC
CLNACC RCV000171453.1,