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rs768384031

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768384031(A;A)
Make rs768384031(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28734517
GeneCHEK2
is asnp
is mentioned by
dbSNPrs768384031
ebirs768384031
HLIrs768384031
Exacrs768384031
Varsomers768384031
Maprs768384031
PheGenIrs768384031
hapmaprs768384031
1000 genomesrs768384031
hgdprs768384031
ensemblrs768384031
gopubmedrs768384031
geneviewrs768384031
scholarrs768384031
googlers768384031
pharmgkbrs768384031
gwascentralrs768384031
openSNPrs768384031
23andMers768384031
23andMe allrs768384031
SNP Nexus

SNPshotrs768384031
SNPdbers768384031
MSV3drs768384031
GWAS Ctlgrs768384031
Max Magnitude0
ClinVar
Risk rs768384031(A,T;A,T)
Alt rs768384031(A,T;A,T)
Reference rs768384031(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene CHEK2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000022.10:g.29130505G>A
CLNSRC
CLNACC RCV000218911.1, RCV000222824.1,