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rs876660250

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660250(-;-)
Make rs876660250(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28699926
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876660250
ebirs876660250
HLIrs876660250
Exacrs876660250
Varsomers876660250
Maprs876660250
PheGenIrs876660250
hapmaprs876660250
1000 genomesrs876660250
hgdprs876660250
ensemblrs876660250
gopubmedrs876660250
geneviewrs876660250
scholarrs876660250
googlers876660250
pharmgkbrs876660250
gwascentralrs876660250
openSNPrs876660250
23andMers876660250
23andMe allrs876660250
SNP Nexus

SNPshotrs876660250
SNPdbers876660250
MSV3drs876660250
GWAS Ctlgrs876660250
Max Magnitude0
ClinVar
Risk rs876660250(;)
Alt rs876660250(;)
Reference rs876660250(G;G)
Significance 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.29095914delC
CLNSRC
CLNACC RCV000219380.1,