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rs148856317

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148856317(C;C)
Make rs148856317(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position31097884
GeneDDX11
is asnp
is mentioned by
dbSNPrs148856317
ebirs148856317
HLIrs148856317
Exacrs148856317
Varsomers148856317
Maprs148856317
PheGenIrs148856317
hapmaprs148856317
1000 genomesrs148856317
hgdprs148856317
ensemblrs148856317
gopubmedrs148856317
geneviewrs148856317
scholarrs148856317
googlers148856317
pharmgkbrs148856317
gwascentralrs148856317
openSNPrs148856317
23andMers148856317
23andMe allrs148856317
SNP Nexus

SNPshotrs148856317
SNPdbers148856317
MSV3drs148856317
GWAS Ctlgrs148856317
Max Magnitude0
ClinVar
Risk rs148856317(C;C)
Alt rs148856317(C;C)
Reference rs148856317(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.31250818G>C
CLNSRC
CLNACC RCV000238763.1,