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rs730881702

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881702(A;A)
Make rs730881702(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28695146
GeneCHEK2
is asnp
is mentioned by
dbSNPrs730881702
ebirs730881702
HLIrs730881702
Exacrs730881702
Varsomers730881702
Maprs730881702
PheGenIrs730881702
hapmaprs730881702
1000 genomesrs730881702
hgdprs730881702
ensemblrs730881702
gopubmedrs730881702
geneviewrs730881702
scholarrs730881702
googlers730881702
pharmgkbrs730881702
gwascentralrs730881702
openSNPrs730881702
23andMers730881702
23andMe allrs730881702
SNP Nexus

SNPshotrs730881702
SNPdbers730881702
MSV3drs730881702
GWAS Ctlgrs730881702
Max Magnitude0
ClinVar
Risk rs730881702(A;A)
Alt rs730881702(A;A)
Reference rs730881702(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29091134C>T
CLNSRC
CLNACC RCV000160453.1,