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- Data Summary
SNP Report
Name | rs7192356 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:83111317(Fwd) | ||
Variant Alleles | G/T | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000539548) intron_variant(ENST00000566620; ENST00000268613; ENST00000565636; ENST00000431540; ENST00000428848; ENST00000539548; ENST00000569454; ENST00000446376) nc_transcript_variant(ENST00000569454) |
||
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.