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

rs1057517777

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517777(C;G)
Make rs1057517777(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position15160995
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs1057517777
dbSNP (old)rs1057517777
ClinGenrs1057517777
ebirs1057517777
HLIrs1057517777
Exacrs1057517777
Gnomadrs1057517777
Varsomers1057517777
LitVarrs1057517777
Maprs1057517777
PheGenIrs1057517777
Biobankrs1057517777
1000 genomesrs1057517777
hgdprs1057517777
ensemblrs1057517777
gopubmedrs1057517777
geneviewrs1057517777
scholarrs1057517777
googlers1057517777
pharmgkbrs1057517777
gwascentralrs1057517777
openSNPrs1057517777
23andMers1057517777
23andMe allrs1057517777
SNPshotrs1057517777
SNPdbers1057517777
MSV3drs1057517777
GWAS Ctlgrs1057517777
Max Magnitude0
ClinVar
Risk rs1057517777(G;G)
Alt rs1057517777(G;G)
Reference Rs1057517777(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NOTCH3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.15271806G>C
CLNSRC
CLNACC RCV000412940.1,