Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521857

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521857(A;C)
Make rs1057521857(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position136510807
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs1057521857
dbSNP (old)rs1057521857
ClinGenrs1057521857
ebirs1057521857
HLIrs1057521857
Exacrs1057521857
Gnomadrs1057521857
Varsomers1057521857
Maprs1057521857
PheGenIrs1057521857
Biobankrs1057521857
1000 genomesrs1057521857
hgdprs1057521857
ensemblrs1057521857
gopubmedrs1057521857
geneviewrs1057521857
scholarrs1057521857
googlers1057521857
pharmgkbrs1057521857
gwascentralrs1057521857
openSNPrs1057521857
23andMers1057521857
23andMe allrs1057521857
SNPshotrs1057521857
SNPdbers1057521857
MSV3drs1057521857
GWAS Ctlgrs1057521857
Max Magnitude0
ClinVar
Risk rs1057521857(C;C)
Alt rs1057521857(C;C)
Reference Rs1057521857(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.139405259T>G
CLNSRC
CLNACC RCV000417942.1,