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rs1064793515

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCTG;TCTG) 0 common in clinvar
Chromosome1
Position119916295
GeneNOTCH2
is asnp
is mentioned by
dbSNPrs1064793515
dbSNP (old)rs1064793515
ClinGenrs1064793515
ebirs1064793515
HLIrs1064793515
Exacrs1064793515
Gnomadrs1064793515
Varsomers1064793515
Maprs1064793515
PheGenIrs1064793515
Biobankrs1064793515
1000 genomesrs1064793515
hgdprs1064793515
ensemblrs1064793515
gopubmedrs1064793515
geneviewrs1064793515
scholarrs1064793515
googlers1064793515
pharmgkbrs1064793515
gwascentralrs1064793515
openSNPrs1064793515
23andMers1064793515
23andMe allrs1064793515
SNPshotrs1064793515
SNPdbers1064793515
MSV3drs1064793515
GWAS Ctlgrs1064793515
Max Magnitude0
ClinVar
Risk rs1064793515(-;-)
Alt rs1064793515(-;-)
Reference Rs1064793515(TCTG;TCTG)
Significance Pathogenic
Disease not provided
Variation info
Gene NOTCH2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.120458918_120458921delCAGA
CLNSRC
CLNACC RCV000480906.1,