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SNP Report
Name | rs6771491 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:51671946 - 51671946(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.0976438 | ||
Functional Annotation | 5_prime_UTR_variant; downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | 5_prime_UTR_variant(ENST00000415259, ENST00000444233, ENST00000457927); downstream_gene_variant(ENST00000409535); intron_variant(ENST00000341333, ENST00000395057, ENST00000412249, ENST00000416589, ENST00000419358, ENST00000425781, ENST00000457573, ENST00000489026, ENST00000493444, ENST00000611400, ENST00000614067); non_coding_transcript_variant(ENST00000489026, ENST00000493444); upstream_gene_variant(ENST00000483429) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |