Have questions? Visit https://www.reddit.com/r/SNPedia

rs560596101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs560596101(A;C)
Make rs560596101(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome22
Position28725241
GeneCHEK2
is asnp
is mentioned by
dbSNPrs560596101
dbSNP (classic)rs560596101
ClinGenrs560596101
ebirs560596101
HLIrs560596101
Exacrs560596101
Gnomadrs560596101
Varsomers560596101
LitVarrs560596101
Maprs560596101
PheGenIrs560596101
Biobankrs560596101
1000 genomesrs560596101
hgdprs560596101
ensemblrs560596101
geneviewrs560596101
scholarrs560596101
googlers560596101
pharmgkbrs560596101
gwascentralrs560596101
openSNPrs560596101
23andMers560596101
23andMe allrs560596101
SNPshotrs560596101
SNPdbers560596101
MSV3drs560596101
GWAS Ctlgrs560596101
Max Magnitude0
ClinVar
Risk rs560596101(C;C) rs560596101(G;G) rs560596101(T;T)
Alt rs560596101(C;C) rs560596101(G;G) rs560596101(T;T)
Reference Rs560596101(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.29121229A>G
CLNSRC
CLNACC RCV000483398.1,