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rs730882048

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882048(-;-)
Make rs730882048(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position152660726
GeneXRCC2
is asnp
is mentioned by
dbSNPrs730882048
ebirs730882048
HLIrs730882048
Exacrs730882048
Varsomers730882048
Maprs730882048
PheGenIrs730882048
hapmaprs730882048
1000 genomesrs730882048
hgdprs730882048
ensemblrs730882048
gopubmedrs730882048
geneviewrs730882048
scholarrs730882048
googlers730882048
pharmgkbrs730882048
gwascentralrs730882048
openSNPrs730882048
23andMers730882048
23andMe allrs730882048
SNP Nexus

SNPshotrs730882048
SNPdbers730882048
MSV3drs730882048
GWAS Ctlgrs730882048
Max Magnitude0
ClinVar
Risk rs730882048(;)
Alt rs730882048(;)
Reference rs730882048(T;T)
Significance Other
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene XRCC2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.152357811delA
CLNSRC
CLNACC RCV000161115.2,