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- Data Summary
SNP Report
Name | rs10011926 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:111026927(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000514184) intron_variant(ENST00000394607; ENST00000302274; ENST00000514184; ENST00000503885; ENST00000506461; ENST00000506625) nc_transcript_variant(ENST00000506461) |
||
No. of Studies | 1 (significant: 0; non-significant: 0; trend: 1) | ||
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.