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- Data Summary
SNP Report
Name | rs2050121 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr1:20016849(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000494342) intron_variant(ENST00000375122; ENST00000294543; ENST00000375127; ENST00000489814) nc_transcript_variant(ENST00000489814) |
||
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.