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rs121965091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121965091(C;C)
Make rs121965091(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position14159826
GeneXPC
is asnp
is mentioned by
dbSNPrs121965091
ebirs121965091
HLIrs121965091
Exacrs121965091
Varsomers121965091
Maprs121965091
PheGenIrs121965091
hapmaprs121965091
1000 genomesrs121965091
hgdprs121965091
ensemblrs121965091
gopubmedrs121965091
geneviewrs121965091
scholarrs121965091
googlers121965091
pharmgkbrs121965091
gwascentralrs121965091
openSNPrs121965091
23andMers121965091
23andMe allrs121965091
SNP Nexus

SNPshotrs121965091
SNPdbers121965091
MSV3drs121965091
GWAS Ctlgrs121965091
Max Magnitude0
ClinVar
Risk rs121965091(C;C)
Alt rs121965091(C;C)
Reference rs121965091(T;T)
Significance Probable-Pathogenic
Disease Malignant tumor of urinary bladder
Variation info
Gene XPC
CLNDBN Malignant tumor of urinary bladder
Reversed 1
HGVS NC_000003.11:g.14201326A>G
CLNSRC
CLNACC


[PMID 21273643OA-icon.png] In vitro functional effects of XPC gene rare variants from bladder cancer patients.

OMIM109800
Desc
Variant
Relatedalso