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Select item 20709841.

rs2070984 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:91179733 (GRCh38)
12:91573510 (GRCh37)
Canonical SPDI:: NC_000012.12:91179732:C:T
Gene:: DCN (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000012.12:g.91179733C>T, NC_000012.11:g.91573510C>T, NG_011672.1:g.8297G>A

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rs2070984 (1)
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