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- Data Summary
SNP Report
Name | rs2253978 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:55911000(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000521228) intron_variant(ENST00000541580; ENST00000518005; ENST00000536025; ENST00000521992; ENST00000521228) nc_transcript_variant(ENST00000541580) upstream_gene_variant(ENST00000520435; ENST00000290567; ENST00000319165) |
||
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.