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rs121965092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965092(A;A)
Make rs121965092(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position14145785
GeneXPC
is asnp
is mentioned by
dbSNPrs121965092
ebirs121965092
HLIrs121965092
Exacrs121965092
Varsomers121965092
Maprs121965092
PheGenIrs121965092
hapmaprs121965092
1000 genomesrs121965092
hgdprs121965092
ensemblrs121965092
gopubmedrs121965092
geneviewrs121965092
scholarrs121965092
googlers121965092
pharmgkbrs121965092
gwascentralrs121965092
openSNPrs121965092
23andMers121965092
23andMe allrs121965092
SNP Nexus

SNPshotrs121965092
SNPdbers121965092
MSV3drs121965092
GWAS Ctlgrs121965092
Max Magnitude0
ClinVar
Risk rs121965092(A;A)
Alt rs121965092(A;A)
Reference rs121965092(G;G)
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.14187285C>T
CLNSRC
CLNACC


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

OMIM109800
Desc
Variant
Relatedalso