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rs1044009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1044009(C;T)
Make rs1044009(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position15160960
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs1044009
dbSNP (classic)rs1044009
ClinGenrs1044009
ebirs1044009
HLIrs1044009
Exacrs1044009
Gnomadrs1044009
Varsomers1044009
LitVarrs1044009
Maprs1044009
PheGenIrs1044009
Biobankrs1044009
1000 genomesrs1044009
hgdprs1044009
ensemblrs1044009
geneviewrs1044009
scholarrs1044009
googlers1044009
pharmgkbrs1044009
gwascentralrs1044009
openSNPrs1044009
23andMers1044009
SNPshotrs1044009
SNPdbers1044009
MSV3drs1044009
GWAS Ctlgrs1044009
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25957329OA-icon.png] Variations in genes involved in dormancy associated with outcome in patients with resected colorectal liver metastases


ClinVar
Risk rs1044009(T;T)
Alt rs1044009(T;T)
Reference Rs1044009(C;C)
Significance Non-pathogenic
Disease not specified Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Variation info
Gene NOTCH3
CLNDBN not specified Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Reversed 1
HGVS NC_000019.9:g.15271771G>A
CLNSRC
CLNACC RCV000249070.2, RCV000278901.1,