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- Data Summary
SNP Report
Name | rs1304100 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:27571603(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000530686; ENST00000500662; ENST00000499568; ENST00000532965; ENST00000501176; ENST00000499008; ENST00000502161) nc_transcript_variant(ENST00000530686; ENST00000500662; ENST00000499568; ENST00000501176; ENST00000499008; ENST00000502161; ENST00000532965) |
||
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.