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- Data Summary
SNP Report
Name | rs10158100 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr1:202394199(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000476364) intron_variant(ENST00000480184; ENST00000406302; ENST00000476364; ENST00000336894; ENST00000356764; ENST00000466968) upstream_gene_variant(ENST00000488330) |
||
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.