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- Data Summary
SNP Report
Basic Info
| Name | rs7812028 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr7:114215804(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000412402; ENST00000441290; ENST00000440349) intron_variant(ENST00000412402; ENST00000441290; ENST00000440349; ENST00000393494; ENST00000408937; ENST00000324462; ENST00000350908; ENST00000459666; ENST00000360232; ENST00000378237; ENST00000393489; ENST00000393498; ENST00000393495; ENST00000452963; ENST00000390668; ENST00000393500; ENST00000403559) nc_transcript_variant(ENST00000459666) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.