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- Data Summary
SNP Report
Name | rs1170101 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr13:42776055(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000261491; ENST00000540693; ENST00000337343; ENST00000379274; ENST00000536612; ENST00000538674; ENST00000498255) nc_transcript_variant(ENST00000498255) |
||
No. of Studies | 1 (significant: 0; non-significant: 1; 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.