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rs560785131

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs560785131(C;T)
Make rs560785131(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position152676040
GeneXRCC2
is asnp
is mentioned by
dbSNPrs560785131
dbSNP (classic)rs560785131
ClinGenrs560785131
ebirs560785131
HLIrs560785131
Exacrs560785131
Gnomadrs560785131
Varsomers560785131
LitVarrs560785131
Maprs560785131
PheGenIrs560785131
Biobankrs560785131
1000 genomesrs560785131
hgdprs560785131
ensemblrs560785131
geneviewrs560785131
scholarrs560785131
googlers560785131
pharmgkbrs560785131
gwascentralrs560785131
openSNPrs560785131
23andMers560785131
23andMe allrs560785131
SNPshotrs560785131
SNPdbers560785131
MSV3drs560785131
GWAS Ctlgrs560785131
Max Magnitude0
ClinVar
Risk rs560785131(T;T)
Alt rs560785131(T;T)
Reference Rs560785131(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene XRCC2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.152373125C>T
CLNSRC
CLNACC RCV000484345.1,