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SNP Report
Name | rs3755485 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:174765825 - 174765825(1) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.371406 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000442996, ENST00000636168); non_coding_transcript_variant(ENST00000442996); upstream_gene_variant(ENST00000261007, ENST00000348749, ENST00000409219, ENST00000409323, ENST00000409542, ENST00000435083) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |