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rs1064795070

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position136518597
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs1064795070
dbSNP (old)rs1064795070
ClinGenrs1064795070
ebirs1064795070
HLIrs1064795070
Exacrs1064795070
Gnomadrs1064795070
Varsomers1064795070
Maprs1064795070
PheGenIrs1064795070
Biobankrs1064795070
1000 genomesrs1064795070
hgdprs1064795070
ensemblrs1064795070
gopubmedrs1064795070
geneviewrs1064795070
scholarrs1064795070
googlers1064795070
pharmgkbrs1064795070
gwascentralrs1064795070
openSNPrs1064795070
23andMers1064795070
23andMe allrs1064795070
SNPshotrs1064795070
SNPdbers1064795070
MSV3drs1064795070
GWAS Ctlgrs1064795070
Max Magnitude0
ClinVar
Risk rs1064795070(T;T)
Alt rs1064795070(T;T)
Reference Rs1064795070(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.139413049G>A
CLNSRC
CLNACC RCV000480413.1,