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- Data Summary
SNP Report
Name | rs3103268 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr2:232984969(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000390005; ENST00000445090; ENST00000433430) intron_variant(ENST00000273009; ENST00000390005; ENST00000409401; ENST00000445090; ENST00000433430; ENST00000470087; ENST00000325385; ENST00000409307; ENST00000360410) nc_transcript_variant(ENST00000470087) |
||
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.