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SNP Report
Name | rs12696671 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:193631130 - 193631130(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.392572 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000392436, ENST00000487986); intron_variant(ENST00000361150, ENST00000361510, ENST00000361715, ENST00000361828, ENST00000361908, ENST00000392438, ENST00000434811, ENST00000495476, ENST00000497189, LRG_337t1, LRG_337t2); non_coding_transcript_variant(ENST00000495476, ENST00000497189); upstream_gene_variant(ENST00000433105, ENST00000444085) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |