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rs121965090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965090(C;T)
Make rs121965090(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position14158706
GeneXPC
is asnp
is mentioned by
dbSNPrs121965090
ebirs121965090
HLIrs121965090
Exacrs121965090
Varsomers121965090
Maprs121965090
PheGenIrs121965090
hapmaprs121965090
1000 genomesrs121965090
hgdprs121965090
ensemblrs121965090
gopubmedrs121965090
geneviewrs121965090
scholarrs121965090
googlers121965090
pharmgkbrs121965090
gwascentralrs121965090
openSNPrs121965090
23andMers121965090
23andMe allrs121965090
SNP Nexus

SNPshotrs121965090
SNPdbers121965090
MSV3drs121965090
GWAS Ctlgrs121965090
Max Magnitude0
ClinVar
Risk rs121965090(T;T)
Alt rs121965090(T;T)
Reference rs121965090(C;C)
Significance Untested
Disease not specified
Variation info
Gene XPC
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.14200206G>A
CLNSRC ClinVar
CLNACC RCV000122342.1,


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

OMIM109800
Desc
Variant
Relatedalso