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rs201968272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201968272(A;A)
Make rs201968272(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position31089147
GeneDDX11
is asnp
is mentioned by
dbSNPrs201968272
ebirs201968272
HLIrs201968272
Exacrs201968272
Varsomers201968272
Maprs201968272
PheGenIrs201968272
hapmaprs201968272
1000 genomesrs201968272
hgdprs201968272
ensemblrs201968272
gopubmedrs201968272
geneviewrs201968272
scholarrs201968272
googlers201968272
pharmgkbrs201968272
gwascentralrs201968272
openSNPrs201968272
23andMers201968272
23andMe allrs201968272
SNP Nexus

SNPshotrs201968272
SNPdbers201968272
MSV3drs201968272
GWAS Ctlgrs201968272
Max Magnitude0
ClinVar
Risk rs201968272(A;A)
Alt rs201968272(A;A)
Reference rs201968272(G;G)
Significance Pathogenic
Disease Warsaw breakage syndrome
Variation info
Gene DDX11
CLNDBN Warsaw breakage syndrome
Reversed 0
HGVS NC_000012.11:g.31242081G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033122.4,