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SNP Report
Name | rs6662982 dbSNP Ensembl | ||
---|---|---|---|
Location | chr1:46411508 - 46411508(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.103035 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000489366, ENST00000493735); intron_variant(ENST00000243167, ENST00000484697, ENST00000493636); NMD_transcript_variant(ENST00000484697); non_coding_transcript_variant(ENST00000493636) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |