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- Data Summary
SNP Report
Name | rs941299 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:73125179(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000462135; ENST00000395156; ENST00000470878; ENST00000222812; ENST00000395155; ENST00000395154) nc_transcript_variant(ENST00000462135; ENST00000470878) upstream_gene_variant(ENST00000578924; ENST00000496216) |
||
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.