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Select item 725513891.

rs72551389 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:68646973 (GRCh38)
4:69512691 (GRCh37)
Canonical SPDI:: NC_000004.12:68646972:G:A,NC_000004.12:68646972:G:C
Gene:: UGT2B15 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000004.12:g.68646973G>A, NC_000004.12:g.68646973G>C, NC_000004.11:g.69512691G>A, NC_000004.11:g.69512691G>C, NG_052676.1:g.28804C>T, NG_052676.1:g.28804C>G, NM_001076.4:c.*131C>T, NM_001076.4:c.*131C>G, NM_001076.3:c.*131C>T, NM_001076.3:c.*131C>G, NT_167250.2:g.223342G>A, NT_167250.2:g.223342G>C, NT_167250.1:g.225292G>A, NT_167250.1:g.225292G>C

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