Have questions? Visit https://www.reddit.com/r/SNPedia

rs540635787

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs540635787(A;A)
Make rs540635787(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28694073
GeneCHEK2
is asnp
is mentioned by
dbSNPrs540635787
ebirs540635787
HLIrs540635787
Exacrs540635787
Varsomers540635787
Maprs540635787
PheGenIrs540635787
hapmaprs540635787
1000 genomesrs540635787
hgdprs540635787
ensemblrs540635787
gopubmedrs540635787
geneviewrs540635787
scholarrs540635787
googlers540635787
pharmgkbrs540635787
gwascentralrs540635787
openSNPrs540635787
23andMers540635787
23andMe allrs540635787
SNP Nexus

SNPshotrs540635787
SNPdbers540635787
MSV3drs540635787
GWAS Ctlgrs540635787
Max Magnitude0
ClinVar
Risk rs540635787(A;A)
Alt rs540635787(A;A)
Reference rs540635787(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not specified Carcinoma of colon Lung cancer Malignant tumor of prostate Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not specified Carcinoma of colon Lung cancer Malignant tumor of prostate Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000022.10:g.29090061G>A; NC_000022.10:g.29090061G>T
CLNSRC
CLNACC RCV000115999.5, RCV000206044.2, RCV000212462.1, RCV000234795.1, RCV000213121.1, RCV000219946.1,