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rs786205516

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205516(A;A)
Make rs786205516(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position14410271
GeneDDX39A
is asnp
is mentioned by
dbSNPrs786205516
ebirs786205516
HLIrs786205516
Exacrs786205516
Varsomers786205516
Maprs786205516
PheGenIrs786205516
hapmaprs786205516
1000 genomesrs786205516
hgdprs786205516
ensemblrs786205516
gopubmedrs786205516
geneviewrs786205516
scholarrs786205516
googlers786205516
pharmgkbrs786205516
gwascentralrs786205516
openSNPrs786205516
23andMers786205516
23andMe allrs786205516
SNP Nexus

SNPshotrs786205516
SNPdbers786205516
MSV3drs786205516
GWAS Ctlgrs786205516
Max Magnitude0
ClinVar
Risk rs786205516(A;A)
Alt rs786205516(A;A)
Reference rs786205516(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDX39A
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.14521083A>T
CLNSRC
CLNACC RCV000171279.1,