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- Data Summary
SNP Report
Name | rs4623937 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:605856(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000534320) intron_variant(ENST00000264555; ENST00000534320; ENST00000532550; ENST00000533464; ENST00000413872; ENST00000416188; ENST00000526724) nc_transcript_variant(ENST00000532550; ENST00000526724) upstream_gene_variant(ENST00000525848) |
||
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.