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rs1064795490

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position70789845
GeneAUTS2
is asnp
is mentioned by
dbSNPrs1064795490
dbSNP (old)rs1064795490
ClinGenrs1064795490
ebirs1064795490
HLIrs1064795490
Exacrs1064795490
Gnomadrs1064795490
Varsomers1064795490
Maprs1064795490
PheGenIrs1064795490
Biobankrs1064795490
1000 genomesrs1064795490
hgdprs1064795490
ensemblrs1064795490
gopubmedrs1064795490
geneviewrs1064795490
scholarrs1064795490
googlers1064795490
pharmgkbrs1064795490
gwascentralrs1064795490
openSNPrs1064795490
23andMers1064795490
23andMe allrs1064795490
SNPshotrs1064795490
SNPdbers1064795490
MSV3drs1064795490
GWAS Ctlgrs1064795490
Max Magnitude0
ClinVar
Risk rs1064795490(-;-)
Alt rs1064795490(-;-)
Reference Rs1064795490(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AUTS2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.70254831delC
CLNSRC
CLNACC RCV000484146.1,