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rs1064793660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position119925359
GeneNOTCH2
is asnp
is mentioned by
dbSNPrs1064793660
dbSNP (old)rs1064793660
ClinGenrs1064793660
ebirs1064793660
HLIrs1064793660
Exacrs1064793660
Gnomadrs1064793660
Varsomers1064793660
LitVarrs1064793660
Maprs1064793660
PheGenIrs1064793660
Biobankrs1064793660
1000 genomesrs1064793660
hgdprs1064793660
ensemblrs1064793660
gopubmedrs1064793660
geneviewrs1064793660
scholarrs1064793660
googlers1064793660
pharmgkbrs1064793660
gwascentralrs1064793660
openSNPrs1064793660
23andMers1064793660
23andMe allrs1064793660
SNPshotrs1064793660
SNPdbers1064793660
MSV3drs1064793660
GWAS Ctlgrs1064793660
Max Magnitude0
ClinVar
Risk rs1064793660(-;-)
Alt rs1064793660(-;-)
Reference Rs1064793660(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NOTCH2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.120467982delG
CLNSRC
CLNACC RCV000481951.1,