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SNP Report
Name | rs11762695 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:7671796 - 7671796(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.04373 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000223129, ENST00000463725, ENST00000469183, ENST00000471760, ENST00000482067, ENST00000493246, ENST00000636849); non_coding_transcript_variant(ENST00000469183, ENST00000471760, ENST00000493246) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |