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- Data Summary
SNP Report
Name | rs11646411 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:82746937(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000569144; ENST00000562601; ENST00000568770; ENST00000539548) intron_variant(ENST00000566620; ENST00000268613; ENST00000569144; ENST00000562601; ENST00000568770; ENST00000565636; ENST00000431540; ENST00000428848; ENST00000539548; ENST00000569455; ENST00000566333; ENST00000567445; ENST00000446376) nc_transcript_variant(ENST00000569455; ENST00000566333) |
||
No. of Studies | 1 (significant: 0; non-significant: 0; trend: 1) | ||
Source | Literature-origin |