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rs3755319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3755319(G;G)
Make rs3755319(G;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position233758936
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs3755319
dbSNP (old)rs3755319
ClinGenrs3755319
ebirs3755319
HLIrs3755319
Exacrs3755319
Gnomadrs3755319
Varsomers3755319
Maprs3755319
PheGenIrs3755319
Biobankrs3755319
1000 genomesrs3755319
hgdprs3755319
ensemblrs3755319
gopubmedrs3755319
geneviewrs3755319
scholarrs3755319
googlers3755319
pharmgkbrs3755319
gwascentralrs3755319
openSNPrs3755319
23andMers3755319
23andMe allrs3755319
SNP Nexus

SNPshotrs3755319
SNPdbers3755319
MSV3drs3755319
GWAS Ctlgrs3755319
Max Magnitude0
? (G;G) (G;T) (T;T) 28


ClinVar
Risk rs3755319(G;G)
Alt rs3755319(G;G)
Reference Rs3755319(T;T)
Significance Pathogenic
Disease Lucey-Driscoll syndrome
Variation info
Gene UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A10 UGT1A8 UGT1A7
CLNDBN Lucey-Driscoll syndrome
Reversed 1
HGVS NC_000002.11:g.234667582A\x3d
CLNSRC OMIM Allelic Variant
CLNACC RCV000013075.17,