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SNP Report
Name | rs268898 dbSNP Ensembl | ||
---|---|---|---|
Location | chr19:50988912 - 50988912(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.467452 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000594512); non_coding_transcript_variant(ENST00000594512); upstream_gene_variant(ENST00000304045, ENST00000593904, ENST00000595638, ENST00000595820, ENST00000597707) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |