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rs6964587

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6964587(G;T)
Make rs6964587(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position92001306
GeneAKAP9
is asnp
is mentioned by
dbSNPrs6964587
ebirs6964587
HLIrs6964587
Exacrs6964587
Varsomers6964587
Maprs6964587
PheGenIrs6964587
hapmaprs6964587
1000 genomesrs6964587
hgdprs6964587
ensemblrs6964587
gopubmedrs6964587
geneviewrs6964587
scholarrs6964587
googlers6964587
pharmgkbrs6964587
gwascentralrs6964587
openSNPrs6964587
23andMers6964587
23andMe allrs6964587
SNP Nexus

SNPshotrs6964587
SNPdbers6964587
MSV3drs6964587
GWAS Ctlgrs6964587
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 26510858] Patients with a high polygenic risk of breast cancer do not have an increased risk of radiotherapy toxicity

ClinVar
Risk rs6964587(T;T)
Alt rs6964587(T;T)
Reference rs6964587(G;G)
Significance Non-pathogenic
Disease not specified Colorectal cancer
Variation info
Gene AKAP9
CLNDBN not specified Colorectal cancer
Reversed 0
HGVS NC_000007.13:g.91630620G>T
CLNSRC
CLNACC RCV000123592.5, RCV000171778.2,