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rs763401560

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGT;AAGT) 0 common in clinvar
Make rs763401560(-;-)
Make rs763401560(-;AAGT)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position152649104
GeneXRCC2
is asnp
is mentioned by
dbSNPrs763401560
dbSNP (classic)rs763401560
ClinGenrs763401560
ebirs763401560
HLIrs763401560
Exacrs763401560
Gnomadrs763401560
Varsomers763401560
LitVarrs763401560
Maprs763401560
PheGenIrs763401560
Biobankrs763401560
1000 genomesrs763401560
hgdprs763401560
ensemblrs763401560
geneviewrs763401560
scholarrs763401560
googlers763401560
pharmgkbrs763401560
gwascentralrs763401560
openSNPrs763401560
23andMers763401560
23andMe allrs763401560
SNPshotrs763401560
SNPdbers763401560
MSV3drs763401560
GWAS Ctlgrs763401560
Max Magnitude0
ClinVar
Risk rs763401560(-;-)
Alt rs763401560(-;-)
Reference Rs763401560(AAGT;AAGT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene XRCC2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.152346189_152346192delAAGT
CLNSRC
CLNACC RCV000481611.1,