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rs869312804

From SNPedia

Merged intors730882048
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312804(-;-)
Make rs869312804(-;T)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position152660727
GeneXRCC2
is asnp
is mentioned by
dbSNPrs869312804
dbSNP (classic)rs869312804
ClinGenrs869312804
ebirs869312804
HLIrs869312804
Exacrs869312804
Gnomadrs869312804
Varsomers869312804
LitVarrs869312804
Maprs869312804
PheGenIrs869312804
Biobankrs869312804
1000 genomesrs869312804
hgdprs869312804
ensemblrs869312804
geneviewrs869312804
scholarrs869312804
googlers869312804
pharmgkbrs869312804
gwascentralrs869312804
openSNPrs869312804
23andMers869312804
23andMe allrs869312804
SNPshotrs869312804
SNPdbers869312804
MSV3drs869312804
GWAS Ctlgrs869312804
StatusMerged into rs730882048
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs869312804(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene XRCC2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000007.13:g.152357811delA
CLNSRC
CLNACC RCV000161115.2, RCV000254696.1,