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- Data Summary
SNP Report
Name | rs1533123 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr2:79898937(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000466387; ENST00000496558; ENST00000409266; ENST00000409971; ENST00000451966; ENST00000402739; ENST00000361291; ENST00000541047; ENST00000540488) | ||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.