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Select item 1355511.

rs135551 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 22:46157126 (GRCh38)
22:46553021 (GRCh37)
Canonical SPDI:: NC_000022.11:46157125:G:A,NC_000022.11:46157125:G:C,NC_000022.11:46157125:G:T
Gene:: PPARA (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.276389/84905 (ALFA)
T=0./0 (KOREAN)
A=0.059759/4628 (TOMMO)
A=0.065386/473 (Korea4K)
A=0.299813/1920 (1000Genomes_30X)
A=0.32981/624 (HapMap)
A=0.335471/50004 (GnomAD_genomes)
A=0.345087/91341 (TOPMED)
A=0.350732/27597 (PAGE_STUDY)
HGVS:: NC_000022.11:g.46157126G>A, NC_000022.11:g.46157126G>C, NC_000022.11:g.46157126G>T, NC_000022.10:g.46553021A>G, NC_000022.10:g.46553021A>C, NC_000022.10:g.46553021A>T, NG_012204.2:g.11593G>A, NG_012204.2:g.11593G>C, NG_012204.2:g.11593G>T

dbSNP