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- Data Summary
SNP Report
Name | rs6466484 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:114012911(Fwd) | ||
Variant Alleles | A/C | ||
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; ENST00000495516; ENST00000324462; ENST00000393500) nc_transcript_variant(ENST00000495516) |
||
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.