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- Data Summary
SNP Report
Name | rs1044396 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr20:61981134(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000498043) NMD_transcript_variant(ENST00000498043) nc_transcript_variant(ENST00000463705; ENST00000467563) non_coding_exon_variant(ENST00000463705; ENST00000467563) synonymous_variant(ENST00000370263) |
||
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.