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- Data Summary
SNP Report
Name | rs6855137 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:91832609(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000505073; ENST00000513522; ENST00000509109) downstream_gene_variant(ENST00000503421) intron_variant(ENST00000505073; ENST00000509176; ENST00000513522; ENST00000509109; ENST00000333691; ENST00000515693) nc_transcript_variant(ENST00000515693) |
||
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.