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rs2227998

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2227998(A;A)
Make rs2227998(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position14152389
GeneXPC
is asnp
is mentioned by
dbSNPrs2227998
ebirs2227998
HLIrs2227998
Exacrs2227998
Varsomers2227998
Maprs2227998
PheGenIrs2227998
hapmaprs2227998
1000 genomesrs2227998
hgdprs2227998
ensemblrs2227998
gopubmedrs2227998
geneviewrs2227998
scholarrs2227998
googlers2227998
pharmgkbrs2227998
gwascentralrs2227998
openSNPrs2227998
23andMers2227998
23andMe allrs2227998
SNP Nexus

SNPshotrs2227998
SNPdbers2227998
MSV3drs2227998
GWAS Ctlgrs2227998
GMAF0.2158
Max Magnitude0

[PMID 21622940OA-icon.png] Single Nucleotide Polymorphisms in DNA Repair Genes and Association with Breast Cancer Risk in the WEB Study

ClinVar
Risk rs2227998(A;A)
Alt rs2227998(A;A)
Reference rs2227998(G;G)
Significance Untested
Disease not specified
Variation info
Gene XPC
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.14193889C>T
CLNSRC ClinVar
CLNACC RCV000122327.1,