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rs730881699

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881699(-;-)
Make rs730881699(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28725282
GeneCHEK2
is asnp
is mentioned by
dbSNPrs730881699
ebirs730881699
HLIrs730881699
Exacrs730881699
Varsomers730881699
Maprs730881699
PheGenIrs730881699
hapmaprs730881699
1000 genomesrs730881699
hgdprs730881699
ensemblrs730881699
gopubmedrs730881699
geneviewrs730881699
scholarrs730881699
googlers730881699
pharmgkbrs730881699
gwascentralrs730881699
openSNPrs730881699
23andMers730881699
23andMe allrs730881699
SNP Nexus

SNPshotrs730881699
SNPdbers730881699
MSV3drs730881699
GWAS Ctlgrs730881699
Max Magnitude0
ClinVar
Risk rs730881699(;)
Alt rs730881699(;)
Reference rs730881699(A;A)
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 1
HGVS NC_000022.10:g.29121270delT
CLNSRC
CLNACC RCV000160449.1, RCV000206058.1,