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rs864622613

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622613(C;C)
Make rs864622613(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28725368
GeneCHEK2
is asnp
is mentioned by
dbSNPrs864622613
ebirs864622613
HLIrs864622613
Exacrs864622613
Varsomers864622613
Maprs864622613
PheGenIrs864622613
hapmaprs864622613
1000 genomesrs864622613
hgdprs864622613
ensemblrs864622613
gopubmedrs864622613
geneviewrs864622613
scholarrs864622613
googlers864622613
pharmgkbrs864622613
gwascentralrs864622613
openSNPrs864622613
23andMers864622613
23andMe allrs864622613
SNP Nexus

SNPshotrs864622613
SNPdbers864622613
MSV3drs864622613
GWAS Ctlgrs864622613
Max Magnitude0
ClinVar
Risk rs864622613(C;C)
Alt rs864622613(C;C)
Reference rs864622613(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29121356C>G
CLNSRC
CLNACC RCV000203880.1,