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Select item 343546691.

rs34354669 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>-,TT,TTT [Show Flanks]
Chromosome:: 2:233668060 (GRCh38)
2:234576706 (GRCh37)
Canonical SPDI:: NC_000002.12:233668059:TTTTTTTTT:TTTTTTTT,NC_000002.12:233668059:TTTTTTTTT:TTTTTTTTTT,NC_000002.12:233668059:TTTTTTTTT:TTTTTTTTTTT
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
T=0.3/12 (GENOME_DK)
T=0.411741/2062 (1000Genomes)
T=0.415033/109855 (TOPMED)
-=0.478333/287 (NorthernSweden)
T=0.479761/1849 (ALSPAC)
T=0.483549/1793 (TWINSUK)
T=0.483705/2167 (Estonian)
HGVS:: NC_000002.12:g.233668068del, NC_000002.12:g.233668068dup, NC_000002.12:g.233668067_233668068dup, NC_000002.11:g.234576714del, NC_000002.11:g.234576714dup, NC_000002.11:g.234576713_234576714dup, NG_002601.2:g.83325del, NG_002601.2:g.83325dup, NG_002601.2:g.83324_83325dup

dbSNP