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- Data Summary
SNP Report
Name | rs1903960 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr10:53721176(Fwd) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000373985; ENST00000373980; ENST00000373976; ENST00000401604) | ||
No. of Studies | 1 (significant: 0; non-significant: 1; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.