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rs1057523819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523819(A;A)
Make rs1057523819(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position136517800
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs1057523819
dbSNP (old)rs1057523819
ClinGenrs1057523819
ebirs1057523819
HLIrs1057523819
Exacrs1057523819
Gnomadrs1057523819
Varsomers1057523819
Maprs1057523819
PheGenIrs1057523819
Biobankrs1057523819
1000 genomesrs1057523819
hgdprs1057523819
ensemblrs1057523819
gopubmedrs1057523819
geneviewrs1057523819
scholarrs1057523819
googlers1057523819
pharmgkbrs1057523819
gwascentralrs1057523819
openSNPrs1057523819
23andMers1057523819
23andMe allrs1057523819
SNPshotrs1057523819
SNPdbers1057523819
MSV3drs1057523819
GWAS Ctlgrs1057523819
Max Magnitude0
ClinVar
Risk rs1057523819(A;A)
Alt rs1057523819(A;A)
Reference Rs1057523819(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.139412252C>T
CLNSRC
CLNACC RCV000434097.1,