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- Data Summary
SNP Report
Name | rs4793927 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:46635019(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000485909; ENST00000490677; ENST00000465846; ENST00000465120; ENST00000464382; ENST00000476342; ENST00000498678; ENST00000460160; ENST00000472863; ENST00000311626; ENST00000489475) nc_transcript_variant(ENST00000464382) upstream_gene_variant(ENST00000471459; ENST00000470495; ENST00000478644) |
||
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.