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rs772683219

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs772683219(-;-)
Make rs772683219(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28703537
GeneCHEK2
is asnp
is mentioned by
dbSNPrs772683219
ebirs772683219
HLIrs772683219
Exacrs772683219
Varsomers772683219
Maprs772683219
PheGenIrs772683219
hapmaprs772683219
1000 genomesrs772683219
hgdprs772683219
ensemblrs772683219
gopubmedrs772683219
geneviewrs772683219
scholarrs772683219
googlers772683219
pharmgkbrs772683219
gwascentralrs772683219
openSNPrs772683219
23andMers772683219
23andMe allrs772683219
SNP Nexus

SNPshotrs772683219
SNPdbers772683219
MSV3drs772683219
GWAS Ctlgrs772683219
Max Magnitude0
ClinVar
Risk rs772683219(;)
Alt rs772683219(;)
Reference rs772683219(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.29099525delA
CLNSRC
CLNACC RCV000215774.1,