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rs768172525

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768172525(C;T)
Make rs768172525(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28696900
GeneCHEK2
is asnp
is mentioned by
dbSNPrs768172525
ebirs768172525
HLIrs768172525
Exacrs768172525
Varsomers768172525
Maprs768172525
PheGenIrs768172525
hapmaprs768172525
1000 genomesrs768172525
hgdprs768172525
ensemblrs768172525
gopubmedrs768172525
geneviewrs768172525
scholarrs768172525
googlers768172525
pharmgkbrs768172525
gwascentralrs768172525
openSNPrs768172525
23andMers768172525
23andMe allrs768172525
SNP Nexus

SNPshotrs768172525
SNPdbers768172525
MSV3drs768172525
GWAS Ctlgrs768172525
Max Magnitude0
ClinVar
Risk rs768172525(T;T)
Alt rs768172525(T;T)
Reference rs768172525(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CHEK2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000022.10:g.29092888C>T
CLNSRC
CLNACC RCV000215927.1,