Have questions? Visit https://www.reddit.com/r/SNPedia

rs1870134

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1870134(C;C)
Make rs1870134(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position14178523
GeneLSM3, XPC
is asnp
is mentioned by
dbSNPrs1870134
ebirs1870134
HLIrs1870134
Exacrs1870134
Varsomers1870134
Maprs1870134
PheGenIrs1870134
hapmaprs1870134
1000 genomesrs1870134
hgdprs1870134
ensemblrs1870134
gopubmedrs1870134
geneviewrs1870134
scholarrs1870134
googlers1870134
pharmgkbrs1870134
gwascentralrs1870134
openSNPrs1870134
23andMers1870134
23andMe allrs1870134
SNP Nexus

SNPshotrs1870134
SNPdbers1870134
MSV3drs1870134
GWAS Ctlgrs1870134
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 26967386] The association of six polymorphisms of five genes involved in three steps of nucleotide excision repair pathways with hepatocellular cancer risk.

ClinVar
Risk rs1870134(C,T;C,T)
Alt rs1870134(C,T;C,T)
Reference rs1870134(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene LSM3 XPC
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.14220023G>C
CLNSRC
CLNACC RCV000122323.2,