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- Data Summary
SNP Report
Name | rs11770199 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:50685602(Fwd) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Functional Annotation | 3_prime_UTR_variant; intron_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000428711) intron_variant(ENST00000407526; ENST00000402497; ENST00000357271; ENST00000406641; ENST00000401949; ENST00000403097; ENST00000402578; ENST00000398812; ENST00000439599; ENST00000335866; ENST00000398810) |
||
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.