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rs1064794088

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome7
Position152649108
GeneXRCC2
is asnp
is mentioned by
dbSNPrs1064794088
dbSNP (old)rs1064794088
ClinGenrs1064794088
ebirs1064794088
HLIrs1064794088
Exacrs1064794088
Gnomadrs1064794088
Varsomers1064794088
Maprs1064794088
PheGenIrs1064794088
Biobankrs1064794088
1000 genomesrs1064794088
hgdprs1064794088
ensemblrs1064794088
gopubmedrs1064794088
geneviewrs1064794088
scholarrs1064794088
googlers1064794088
pharmgkbrs1064794088
gwascentralrs1064794088
openSNPrs1064794088
23andMers1064794088
23andMe allrs1064794088
SNPshotrs1064794088
SNPdbers1064794088
MSV3drs1064794088
GWAS Ctlgrs1064794088
Max Magnitude0
ClinVar
Risk rs1064794088(A;A)
Alt rs1064794088(A;A)
Reference Rs1064794088(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene XRCC2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.152346193A>T
CLNSRC
CLNACC RCV000480672.1,