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Select item 357136351.

rs35713635 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 2:233643842 (GRCh38)
2:234552489 (GRCh37)
Canonical SPDI:: NC_000002.12:233643842::A
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000002.12:g.233643842_233643843insA, NC_000002.11:g.234552488_234552489insA, NG_002601.2:g.59099_59100insA

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35713635[uid] (1)
SNP
71423607[uid] (1)
SNP
45464594[uid] (1)
SNP
72984472[uid] (1)
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ENSSSCG00000000992 AND (alive[prop]) (0)
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