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rs1050411259

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1050411259(A;T)
Make rs1050411259(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position24278081
GeneDCDC2
is asnp
is mentioned by
dbSNPrs1050411259
dbSNP (old)rs1050411259
ClinGenrs1050411259
ebirs1050411259
HLIrs1050411259
Exacrs1050411259
Gnomadrs1050411259
Varsomers1050411259
Maprs1050411259
PheGenIrs1050411259
Biobankrs1050411259
1000 genomesrs1050411259
hgdprs1050411259
ensemblrs1050411259
gopubmedrs1050411259
geneviewrs1050411259
scholarrs1050411259
googlers1050411259
pharmgkbrs1050411259
gwascentralrs1050411259
openSNPrs1050411259
23andMers1050411259
23andMe allrs1050411259
SNP Nexus

SNPshotrs1050411259
SNPdbers1050411259
MSV3drs1050411259
GWAS Ctlgrs1050411259
Max Magnitude0
ClinVar
Risk rs1050411259(T;T)
Alt rs1050411259(T;T)
Reference Rs1050411259(A;A)
Significance Pathogenic
Disease Sclerosing cholangitis
Variation info
Gene DCDC2
CLNDBN Sclerosing cholangitis, neonatal
Reversed 0
HGVS NC_000006.11:g.24278309A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477711.1,