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rs1057518096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACA;ACA) 0 common in clinvar
Make rs1057518096(-;-)
Make rs1057518096(-;ACA)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position136498901
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs1057518096
dbSNP (old)rs1057518096
ClinGenrs1057518096
ebirs1057518096
HLIrs1057518096
Exacrs1057518096
Gnomadrs1057518096
Varsomers1057518096
Maprs1057518096
PheGenIrs1057518096
Biobankrs1057518096
1000 genomesrs1057518096
hgdprs1057518096
ensemblrs1057518096
gopubmedrs1057518096
geneviewrs1057518096
scholarrs1057518096
googlers1057518096
pharmgkbrs1057518096
gwascentralrs1057518096
openSNPrs1057518096
23andMers1057518096
23andMe allrs1057518096
SNPshotrs1057518096
SNPdbers1057518096
MSV3drs1057518096
GWAS Ctlgrs1057518096
Max Magnitude0
ClinVar
Risk rs1057518096(-;-)
Alt rs1057518096(-;-)
Reference Rs1057518096(ACA;ACA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.139393353_139393355delTGT
CLNSRC
CLNACC RCV000413535.1,