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rs876659422

From SNPedia

Orientationminus
Geno Mag Summary
(GCACGTTTTACG;GCACGTTTTACG) 0 common in clinvar
Make rs876659422(-;-)
Make rs876659422(-;GCACGTTTTACG)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28694065
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659422
ebirs876659422
HLIrs876659422
Exacrs876659422
Varsomers876659422
Maprs876659422
PheGenIrs876659422
hapmaprs876659422
1000 genomesrs876659422
hgdprs876659422
ensemblrs876659422
gopubmedrs876659422
geneviewrs876659422
scholarrs876659422
googlers876659422
pharmgkbrs876659422
gwascentralrs876659422
openSNPrs876659422
23andMers876659422
23andMe allrs876659422
SNP Nexus

SNPshotrs876659422
SNPdbers876659422
MSV3drs876659422
GWAS Ctlgrs876659422
Max Magnitude0
ClinVar
Risk rs876659422(;)
Alt rs876659422(;)
Reference rs876659422(GCACGTTTTACG;GCACGTTTTACG)
Significance Probable-Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CHEK2
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000022.10:g.29090053_29090064delCGTAAAACGTGC
CLNSRC
CLNACC RCV000220927.1, RCV000223426.1,