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- Data Summary
SNP Report
Name | rs8636 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr20:10287742(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | 3_prime_UTR_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000254976; ENST00000304886) intron_variant(ENST00000453544; ENST00000421143) nc_transcript_variant(ENST00000421143; ENST00000453544; ENST00000495883) non_coding_exon_variant(ENST00000495883) |
||
No. of Studies | 4 (significant: 2; non-significant: 2; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.