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rs755218546

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755218546(A;A)
Make rs755218546(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position233767936
GeneUGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10
is asnp
is mentioned by
dbSNPrs755218546
dbSNP (classic)rs755218546
ClinGenrs755218546
ebirs755218546
HLIrs755218546
Exacrs755218546
Gnomadrs755218546
Varsomers755218546
LitVarrs755218546
Maprs755218546
PheGenIrs755218546
Biobankrs755218546
1000 genomesrs755218546
hgdprs755218546
ensemblrs755218546
geneviewrs755218546
scholarrs755218546
googlers755218546
pharmgkbrs755218546
gwascentralrs755218546
openSNPrs755218546
23andMers755218546
23andMe allrs755218546
SNPshotrs755218546
SNPdbers755218546
MSV3drs755218546
GWAS Ctlgrs755218546
Max Magnitude0
ClinVar
Risk rs755218546(A;A)
Alt rs755218546(A;A)
Reference Rs755218546(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene UGT1A5 UGT1A3 UGT1A9 UGT1A6 UGT1A4 UGT1A1 UGT1A8 UGT1A10 UGT1A7
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.234676582G>A
CLNSRC
CLNACC RCV000482866.1,