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- Data Summary
SNP Report
Name | rs580237 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:112194032(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000520401) intron_variant(ENST00000520401) upstream_gene_variant(ENST00000506987; ENST00000506997; ENST00000515755; ENST00000282999; ENST00000515463; ENST00000445150; ENST00000509024; ENST00000503445; ENST00000512790; ENST00000505459) |
||
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.