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rs2369049

From SNPedia

Orientationplus
Stabilizedplus
Make rs2369049(A;A)
Make rs2369049(A;G)
Make rs2369049(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position95705514
is asnp
is mentioned by
dbSNPrs2369049
ebirs2369049
HLIrs2369049
Exacrs2369049
Varsomers2369049
Maprs2369049
PheGenIrs2369049
hapmaprs2369049
1000 genomesrs2369049
hgdprs2369049
ensemblrs2369049
gopubmedrs2369049
geneviewrs2369049
scholarrs2369049
googlers2369049
pharmgkbrs2369049
gwascentralrs2369049
openSNPrs2369049
23andMers2369049
23andMe allrs2369049
SNP Nexus

SNPshotrs2369049
SNPdbers2369049
MSV3drs2369049
GWAS Ctlgrs2369049
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