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rs587780170

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780170(C;C)
Make rs587780170(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28695786
GeneCHEK2
is asnp
is mentioned by
dbSNPrs587780170
dbSNP (classic)rs587780170
ClinGenrs587780170
ebirs587780170
HLIrs587780170
Exacrs587780170
Gnomadrs587780170
Varsomers587780170
LitVarrs587780170
Maprs587780170
PheGenIrs587780170
Biobankrs587780170
1000 genomesrs587780170
hgdprs587780170
ensemblrs587780170
geneviewrs587780170
scholarrs587780170
googlers587780170
pharmgkbrs587780170
gwascentralrs587780170
openSNPrs587780170
23andMers587780170
23andMe allrs587780170
SNPshotrs587780170
SNPdbers587780170
MSV3drs587780170
GWAS Ctlgrs587780170
Max Magnitude0
ClinVar
Risk rs587780170(A;A) rs587780170(C;C) rs587780170(T;T)
Alt rs587780170(A;A) rs587780170(C;C) rs587780170(T;T)
Reference Rs587780170(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of breast Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Neoplasm of breast Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29091774C>A; NC_000022.10:g.29091774C>G; NC_000022.10:g.29091774C>T
CLNSRC
CLNACC RCV000422650.1, RCV000115987.6, RCV000212454.2, RCV000230538.2, RCV000467802.1,