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- Data Summary
SNP Report
Name | rs174549 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:61571382(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Functional Annotation | 5_prime_UTR_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000460649) intron_variant(ENST00000574708; ENST00000433932; ENST00000542506; ENST00000539999; ENST00000496123; ENST00000350997; ENST00000536991) nc_transcript_variant(ENST00000496123) |
||
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.