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rs545982789

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs545982789(A;G)
Make rs545982789(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28711907
GeneCHEK2
is asnp
is mentioned by
dbSNPrs545982789
ebirs545982789
HLIrs545982789
Exacrs545982789
Varsomers545982789
Maprs545982789
PheGenIrs545982789
hapmaprs545982789
1000 genomesrs545982789
hgdprs545982789
ensemblrs545982789
gopubmedrs545982789
geneviewrs545982789
scholarrs545982789
googlers545982789
pharmgkbrs545982789
gwascentralrs545982789
openSNPrs545982789
23andMers545982789
23andMe allrs545982789
SNP Nexus

SNPshotrs545982789
SNPdbers545982789
MSV3drs545982789
GWAS Ctlgrs545982789
Max Magnitude0
ClinVar
Risk rs545982789(G;G)
Alt rs545982789(G;G)
Reference rs545982789(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000022.10:g.29107895A>G
CLNSRC
CLNACC RCV000205137.1,