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rs143153871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143153871(A;A)
Make rs143153871(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position152648842
GeneXRCC2
is asnp
is mentioned by
dbSNPrs143153871
dbSNP (classic)rs143153871
ClinGenrs143153871
ebirs143153871
HLIrs143153871
Exacrs143153871
Gnomadrs143153871
Varsomers143153871
LitVarrs143153871
Maprs143153871
PheGenIrs143153871
Biobankrs143153871
1000 genomesrs143153871
hgdprs143153871
ensemblrs143153871
geneviewrs143153871
scholarrs143153871
googlers143153871
pharmgkbrs143153871
gwascentralrs143153871
openSNPrs143153871
23andMers143153871
23andMe allrs143153871
SNPshotrs143153871
SNPdbers143153871
MSV3drs143153871
GWAS Ctlgrs143153871
Max Magnitude0
ClinVar
Risk rs143153871(A;A)
Alt rs143153871(A;A)
Reference Rs143153871(G;G)
Significance Pathogenic
Disease Variant of unknown significance Hereditary cancer-predisposing syndrome not specified
Variation info
Gene XRCC2
CLNDBN Variant of unknown significance Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000007.13:g.152345927G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022966.5, RCV000210083.1, RCV000236424.1,