Have questions? Visit https://www.reddit.com/r/SNPedia

rs587780129

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780129(-;-)
Make rs587780129(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position152648940
GeneXRCC2
is asnp
is mentioned by
dbSNPrs587780129
ebirs587780129
HLIrs587780129
Exacrs587780129
Varsomers587780129
Maprs587780129
PheGenIrs587780129
hapmaprs587780129
1000 genomesrs587780129
hgdprs587780129
ensemblrs587780129
gopubmedrs587780129
geneviewrs587780129
scholarrs587780129
googlers587780129
pharmgkbrs587780129
gwascentralrs587780129
openSNPrs587780129
23andMers587780129
23andMe allrs587780129
SNP Nexus

SNPshotrs587780129
SNPdbers587780129
MSV3drs587780129
GWAS Ctlgrs587780129
Max Magnitude0
ClinVar
Risk rs587780129(;)
Alt rs587780129(;)
Reference rs587780129(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene XRCC2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.152346025delT
CLNSRC
CLNACC RCV000115892.2,