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rs1057519101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519101(C;T)
Make rs1057519101(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position15185371
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs1057519101
dbSNP (old)rs1057519101
ClinGenrs1057519101
ebirs1057519101
HLIrs1057519101
Exacrs1057519101
Gnomadrs1057519101
Varsomers1057519101
LitVarrs1057519101
Maprs1057519101
PheGenIrs1057519101
Biobankrs1057519101
1000 genomesrs1057519101
hgdprs1057519101
ensemblrs1057519101
gopubmedrs1057519101
geneviewrs1057519101
scholarrs1057519101
googlers1057519101
pharmgkbrs1057519101
gwascentralrs1057519101
openSNPrs1057519101
23andMers1057519101
23andMe allrs1057519101
SNPshotrs1057519101
SNPdbers1057519101
MSV3drs1057519101
GWAS Ctlgrs1057519101
Max Magnitude0
ClinVar
Risk rs1057519101(T;T)
Alt rs1057519101(T;T)
Reference Rs1057519101(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOTCH3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.15296182G>A
CLNSRC
CLNACC RCV000416179.1,