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rs774175654

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774175654(-;-)
Make rs774175654(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28689188
GeneCHEK2
is asnp
is mentioned by
dbSNPrs774175654
ebirs774175654
HLIrs774175654
Exacrs774175654
Varsomers774175654
Maprs774175654
PheGenIrs774175654
hapmaprs774175654
1000 genomesrs774175654
hgdprs774175654
ensemblrs774175654
gopubmedrs774175654
geneviewrs774175654
scholarrs774175654
googlers774175654
pharmgkbrs774175654
gwascentralrs774175654
openSNPrs774175654
23andMers774175654
23andMe allrs774175654
SNP Nexus

SNPshotrs774175654
SNPdbers774175654
MSV3drs774175654
GWAS Ctlgrs774175654
Max Magnitude0
ClinVar
Risk rs774175654(;)
Alt rs774175654(;)
Reference rs774175654(C;C)
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.29085176delC
CLNSRC
CLNACC RCV000164545.1, RCV000226984.1,