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- Data Summary
SNP Report
Name | rs911191 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr6:155152311(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Functional Annotation | intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000367178; ENST00000367186; ENST00000417268) upstream_gene_variant(ENST00000460692; ENST00000461783; ENST00000535064) |
||
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.