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rs7159713

From SNPedia

Orientationplus
Stabilizedplus
Make rs7159713(A;A)
Make rs7159713(A;G)
Make rs7159713(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position95703240
is asnp
is mentioned by
dbSNPrs7159713
ebirs7159713
HLIrs7159713
Exacrs7159713
Varsomers7159713
Maprs7159713
PheGenIrs7159713
hapmaprs7159713
1000 genomesrs7159713
hgdprs7159713
ensemblrs7159713
gopubmedrs7159713
geneviewrs7159713
scholarrs7159713
googlers7159713
pharmgkbrs7159713
gwascentralrs7159713
openSNPrs7159713
23andMers7159713
23andMe allrs7159713
SNP Nexus

SNPshotrs7159713
SNPdbers7159713
MSV3drs7159713
GWAS Ctlgrs7159713
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25035853OA-icon.png] Genotype, allele and haplotype frequencies of four TCL1A gene polymorphisms associated with musculoskeletal toxicity in the South Indian descent