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rs200275281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200275281(C;G)
Make rs200275281(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position39504079
GeneDLL3
is asnp
is mentioned by
dbSNPrs200275281
dbSNP (classic)rs200275281
ClinGenrs200275281
ebirs200275281
HLIrs200275281
Exacrs200275281
Gnomadrs200275281
Varsomers200275281
LitVarrs200275281
Maprs200275281
PheGenIrs200275281
Biobankrs200275281
1000 genomesrs200275281
hgdprs200275281
ensemblrs200275281
geneviewrs200275281
scholarrs200275281
googlers200275281
pharmgkbrs200275281
gwascentralrs200275281
openSNPrs200275281
23andMers200275281
SNPshotrs200275281
SNPdbers200275281
MSV3drs200275281
GWAS Ctlgrs200275281
Max Magnitude0
ClinVar
Risk rs200275281(G;G) rs200275281(T;T)
Alt rs200275281(G;G) rs200275281(T;T)
Reference Rs200275281(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DLL3
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.39994719C>T
CLNSRC
CLNACC RCV000426077.1,