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rs760502479

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760502479(G;T)
Make rs760502479(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28696985
GeneCHEK2
is asnp
is mentioned by
dbSNPrs760502479
ebirs760502479
HLIrs760502479
Exacrs760502479
Varsomers760502479
Maprs760502479
PheGenIrs760502479
hapmaprs760502479
1000 genomesrs760502479
hgdprs760502479
ensemblrs760502479
gopubmedrs760502479
geneviewrs760502479
scholarrs760502479
googlers760502479
pharmgkbrs760502479
gwascentralrs760502479
openSNPrs760502479
23andMers760502479
23andMe allrs760502479
SNP Nexus

SNPshotrs760502479
SNPdbers760502479
MSV3drs760502479
GWAS Ctlgrs760502479
Max Magnitude0
ClinVar
Risk rs760502479(T;T)
Alt rs760502479(T;T)
Reference rs760502479(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000022.10:g.29092973G>T
CLNSRC
CLNACC RCV000164779.1,