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- Data Summary
SNP Report
Name | rs10052184 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:175298874(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Functional Annotation | 5_prime_UTR_variant; intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000514150) intron_variant(ENST00000359546; ENST00000512824; ENST00000509837; ENST00000515502; ENST00000393745) upstream_gene_variant(ENST00000502265) |
||
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.