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rs761494650

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761494650(A;A)
Make rs761494650(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28734637
GeneCHEK2
is asnp
is mentioned by
dbSNPrs761494650
ebirs761494650
HLIrs761494650
Exacrs761494650
Varsomers761494650
Maprs761494650
PheGenIrs761494650
hapmaprs761494650
1000 genomesrs761494650
hgdprs761494650
ensemblrs761494650
gopubmedrs761494650
geneviewrs761494650
scholarrs761494650
googlers761494650
pharmgkbrs761494650
gwascentralrs761494650
openSNPrs761494650
23andMers761494650
23andMe allrs761494650
SNP Nexus

SNPshotrs761494650
SNPdbers761494650
MSV3drs761494650
GWAS Ctlgrs761494650
Max Magnitude0
ClinVar
Risk rs761494650(A;A)
Alt rs761494650(A;A)
Reference rs761494650(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 0
HGVS NC_000022.10:g.29130625G>A
CLNSRC Inc.
CLNACC RCV000167444.2, RCV000228262.1,