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- Data Summary
SNP Report
Name | rs1042098 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:1394815(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | 3_prime_UTR_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000512002; ENST00000270349; ENST00000453492) | ||
No. of Studies | 2 (significant: 1; 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.