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SNP Report
Name | rs11223703 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:134125356 - 134125356(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.154353 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000299106, ENST00000441717, ENST00000531302, ENST00000532252, ENST00000534549); NMD_transcript_variant(ENST00000532252); non_coding_transcript_variant(ENST00000531302); upstream_gene_variant(ENST00000524969, ENST00000534330) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |