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rs536907995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs536907995(A;A)
Make rs536907995(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome22
Position28734664
GeneCHEK2
is asnp
is mentioned by
dbSNPrs536907995
dbSNP (classic)rs536907995
ClinGenrs536907995
ebirs536907995
HLIrs536907995
Exacrs536907995
Gnomadrs536907995
Varsomers536907995
LitVarrs536907995
Maprs536907995
PheGenIrs536907995
Biobankrs536907995
1000 genomesrs536907995
hgdprs536907995
ensemblrs536907995
geneviewrs536907995
scholarrs536907995
googlers536907995
pharmgkbrs536907995
gwascentralrs536907995
openSNPrs536907995
23andMers536907995
23andMe allrs536907995
SNPshotrs536907995
SNPdbers536907995
MSV3drs536907995
GWAS Ctlgrs536907995
Max Magnitude0
ClinVar
Risk rs536907995(A;A)
Alt rs536907995(A;A)
Reference Rs536907995(G;G)
Significance Pathogenic
Disease not specified not provided Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN not specified not provided Familial cancer of breast
Reversed 0
HGVS NC_000022.10:g.29130652G>A
CLNSRC
CLNACC RCV000120552.1, RCV000255024.1, RCV000458969.1,