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rs876659838

From SNPedia

Orientationminus
Geno Mag Summary
(TAGATT;TAGATT) 0 common in clinvar
Make rs876659838(-;-)
Make rs876659838(-;TAGATT)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28695871
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659838
ebirs876659838
HLIrs876659838
Exacrs876659838
Varsomers876659838
Maprs876659838
PheGenIrs876659838
hapmaprs876659838
1000 genomesrs876659838
hgdprs876659838
ensemblrs876659838
gopubmedrs876659838
geneviewrs876659838
scholarrs876659838
googlers876659838
pharmgkbrs876659838
gwascentralrs876659838
openSNPrs876659838
23andMers876659838
23andMe allrs876659838
SNP Nexus

SNPshotrs876659838
SNPdbers876659838
MSV3drs876659838
GWAS Ctlgrs876659838
Max Magnitude0
ClinVar
Risk rs876659838(;)
Alt rs876659838(;)
Reference rs876659838(TAGATT;TAGATT)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CHEK2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000022.10:g.29091859_29091864delAATCTA
CLNSRC
CLNACC RCV000213840.1,