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Select item 729844721.

rs72984472 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:233643575 (GRCh38)
2:234552221 (GRCh37)
Canonical SPDI:: NC_000002.12:233643574:C:G
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000416/6 (ALFA)
G=0.000214/30 (GnomAD)
G=0.000291/77 (TOPMED)
G=0.000312/2 (1000Genomes)
G=0.000519/2 (ALSPAC)
G=0.000539/2 (TWINSUK)
HGVS:: NC_000002.12:g.233643575C>G, NC_000002.11:g.234552221C>G, NG_002601.2:g.58832C>G

72984472[uid] (1)
SNP
ENSSSCG00000000992 AND (alive[prop]) (0)
Gene
2123622[uid] (1)
SNP
HOXD1 [Mustela putorius furo]
HOXD1 [Mustela putorius furo]
Gene ID:101670119

Gene
Sequence 427 from Patent WO0123604
Sequence 427 from Patent WO0123604
gi|13924898|emb|AX109694.1||pat|WO| 04|427

Nucleotide

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