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rs207906

From SNPedia

Orientationplus
Stabilizedplus
Make rs207906(A;A)
Make rs207906(A;G)
Make rs207906(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position216148178
GeneXRCC5
is asnp
is mentioned by
dbSNPrs207906
ebirs207906
HLIrs207906
Exacrs207906
Varsomers207906
Maprs207906
PheGenIrs207906
hapmaprs207906
1000 genomesrs207906
hgdprs207906
ensemblrs207906
gopubmedrs207906
geneviewrs207906
scholarrs207906
googlers207906
pharmgkbrs207906
gwascentralrs207906
openSNPrs207906
23andMers207906
23andMe allrs207906
SNP Nexus

SNPshotrs207906
SNPdbers207906
MSV3drs207906
GWAS Ctlgrs207906
GMAF0.1065
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21346221] Risk of acute promyelocytic leukemia in multiple sclerosis: Coding variants of DNA repair genes


[PMID 24615081] Association of XRCC5 polymorphisms with COPD and COPD-related phenotypes in the Han Chinese population: a case-control cohort study.