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- Data Summary
SNP Report
Basic Info
| Name | rs9291412 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr4:20727464(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000471979; ENST00000506702; ENST00000467997; ENST00000508952) downstream_gene_variant(ENST00000382148; ENST00000506552; ENST00000506951; ENST00000447367; ENST00000382150; ENST00000413487; ENST00000382152; ENST00000382149; ENST00000509207; ENST00000515786; ENST00000359001) intron_variant(ENST00000507634; ENST00000503585; ENST00000502938; ENST00000295290; ENST00000471979; ENST00000513459; ENST00000538990; ENST00000502374; ENST00000444671; ENST00000360916; ENST00000506648; ENST00000506702; ENST00000467997; ENST00000508952) nc_transcript_variant(ENST00000506648) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.