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rs904944428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs904944428(-;T)
Make rs904944428(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position24301742
GeneDCDC2
is asnp
is mentioned by
dbSNPrs904944428
dbSNP (classic)rs904944428
ClinGenrs904944428
ebirs904944428
HLIrs904944428
Exacrs904944428
Gnomadrs904944428
Varsomers904944428
LitVarrs904944428
Maprs904944428
PheGenIrs904944428
Biobankrs904944428
1000 genomesrs904944428
hgdprs904944428
ensemblrs904944428
geneviewrs904944428
scholarrs904944428
googlers904944428
pharmgkbrs904944428
gwascentralrs904944428
openSNPrs904944428
23andMers904944428
23andMe allrs904944428
SNPshotrs904944428
SNPdbers904944428
MSV3drs904944428
GWAS Ctlgrs904944428
Max Magnitude0
ClinVar
Risk rs904944428(T;T)
Alt rs904944428(T;T)
Reference Rs904944428(-;-)
Significance Pathogenic
Disease Sclerosing cholangitis
Variation info
Gene DCDC2
CLNDBN Sclerosing cholangitis, neonatal
Reversed 0
HGVS NC_000006.11:g.24301971dup
CLNSRC OMIM Allelic Variant
CLNACC RCV000477740.1,