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rs371418985

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371418985(C;T)
Make rs371418985(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28695737
GeneCHEK2
is asnp
is mentioned by
dbSNPrs371418985
ebirs371418985
HLIrs371418985
Exacrs371418985
Varsomers371418985
Maprs371418985
PheGenIrs371418985
hapmaprs371418985
1000 genomesrs371418985
hgdprs371418985
ensemblrs371418985
gopubmedrs371418985
geneviewrs371418985
scholarrs371418985
googlers371418985
pharmgkbrs371418985
gwascentralrs371418985
openSNPrs371418985
23andMers371418985
23andMe allrs371418985
SNP Nexus

SNPshotrs371418985
SNPdbers371418985
MSV3drs371418985
GWAS Ctlgrs371418985
Max Magnitude0
ClinVar
Risk rs371418985(T;T)
Alt rs371418985(T;T)
Reference rs371418985(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.29091725C>T
CLNSRC
CLNACC RCV000220219.1,