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rs786205519

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205519(A;A)
Make rs786205519(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position39507081
GeneDLL3
is asnp
is mentioned by
dbSNPrs786205519
ebirs786205519
HLIrs786205519
Exacrs786205519
Varsomers786205519
Maprs786205519
PheGenIrs786205519
hapmaprs786205519
1000 genomesrs786205519
hgdprs786205519
ensemblrs786205519
gopubmedrs786205519
geneviewrs786205519
scholarrs786205519
googlers786205519
pharmgkbrs786205519
gwascentralrs786205519
openSNPrs786205519
23andMers786205519
23andMe allrs786205519
SNP Nexus

SNPshotrs786205519
SNPdbers786205519
MSV3drs786205519
GWAS Ctlgrs786205519
Max Magnitude0
ClinVar
Risk rs786205519(A;A)
Alt rs786205519(A;A)
Reference rs786205519(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DLL3
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.39997721G>A
CLNSRC
CLNACC RCV000171283.1,