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SNP Report
Name | rs1295101 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:5996108 - 5996108(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.401757 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000378092, ENST00000378097, ENST00000378111, ENST00000445501, ENST00000478098, ENST00000493807); non_coding_transcript_variant(ENST00000478098, ENST00000493807); upstream_gene_variant(ENST00000378156, ENST00000378169, ENST00000478423, ENST00000489180, ENST00000622020) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |