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rs1871922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
Make rs1871922(A;C)
Make rs1871922(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position129183756
GeneCNBP
is asnp
is mentioned by
dbSNPrs1871922
ebirs1871922
HLIrs1871922
Exacrs1871922
Varsomers1871922
Maprs1871922
PheGenIrs1871922
hapmaprs1871922
1000 genomesrs1871922
hgdprs1871922
ensemblrs1871922
gopubmedrs1871922
geneviewrs1871922
scholarrs1871922
googlers1871922
pharmgkbrs1871922
gwascentralrs1871922
openSNPrs1871922
23andMers1871922
23andMe allrs1871922
SNP Nexus

SNPshotrs1871922
SNPdbers1871922
MSV3drs1871922
GWAS Ctlgrs1871922
GMAF0.4555
Max Magnitude0

[PMID 21224892OA-icon.png] Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype[PMID 12970845OA-icon.png] Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.

[PMID 19020295OA-icon.png] Premutation allele pool in myotonic dystrophy type 2.