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- Data Summary
SNP Report
Name | rs2189790 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:63644270(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000581734) intron_variant(ENST00000535342; ENST00000581739; ENST00000583466; ENST00000580694; ENST00000537949; ENST00000582795; ENST00000581734; ENST00000317442; ENST00000392769; ENST00000541355) nc_transcript_variant(ENST00000583466; ENST00000580694; ENST00000582795) |
||
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.