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rs1064794965

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome22
Position28695826
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1064794965
dbSNP (old)rs1064794965
ClinGenrs1064794965
ebirs1064794965
HLIrs1064794965
Exacrs1064794965
Gnomadrs1064794965
Varsomers1064794965
Maprs1064794965
PheGenIrs1064794965
Biobankrs1064794965
1000 genomesrs1064794965
hgdprs1064794965
ensemblrs1064794965
gopubmedrs1064794965
geneviewrs1064794965
scholarrs1064794965
googlers1064794965
pharmgkbrs1064794965
gwascentralrs1064794965
openSNPrs1064794965
23andMers1064794965
23andMe allrs1064794965
SNPshotrs1064794965
SNPdbers1064794965
MSV3drs1064794965
GWAS Ctlgrs1064794965
Max Magnitude0
ClinVar
Risk rs1064794965(A;A)
Alt rs1064794965(A;A)
Reference Rs1064794965(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29091814_29091815insT
CLNSRC
CLNACC RCV000482812.1,