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rs1064793566

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TATA;TATA) 0 common in clinvar
Chromosome22
Position28696904
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1064793566
dbSNP (old)rs1064793566
ClinGenrs1064793566
ebirs1064793566
HLIrs1064793566
Exacrs1064793566
Gnomadrs1064793566
Varsomers1064793566
Maprs1064793566
PheGenIrs1064793566
Biobankrs1064793566
1000 genomesrs1064793566
hgdprs1064793566
ensemblrs1064793566
gopubmedrs1064793566
geneviewrs1064793566
scholarrs1064793566
googlers1064793566
pharmgkbrs1064793566
gwascentralrs1064793566
openSNPrs1064793566
23andMers1064793566
23andMe allrs1064793566
SNPshotrs1064793566
SNPdbers1064793566
MSV3drs1064793566
GWAS Ctlgrs1064793566
Max Magnitude0
ClinVar
Risk rs1064793566(-;-)
Alt rs1064793566(-;-)
Reference Rs1064793566(TATA;TATA)
Significance Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29092892_29092895delTATA
CLNSRC
CLNACC RCV000485854.1,