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Select item 6270991.

rs627099 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 18:42073259 (GRCh38)
18:39653223 (GRCh37)
Canonical SPDI:: NC_000018.10:42073258:C:A,NC_000018.10:42073258:C:G,NC_000018.10:42073258:C:T
Gene:: PIK3C3 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.129086/1627 (ALFA)
G=0.2/8 (GENOME_DK)
G=0.208259/933 (Estonian)
G=0.239479/239 (GoNL)
G=0.241667/145 (NorthernSweden)
G=0.251348/932 (TWINSUK)
G=0.254281/980 (ALSPAC)
G=0.31269/2262 (Korea4K)
G=0.325328/596 (Korea1K)
G=0.327645/960 (KOREAN)
G=0.346843/91806 (TOPMED)
G=0.352381/74 (Vietnamese)
G=0.38139/1910 (1000Genomes)
G=0.381793/2445 (1000Genomes_30X)
C=0.391176/133 (SGDP_PRJ)
G=0.408537/134 (HapMap)
C=0.409091/9 (Siberian)
G=0.421296/91 (Qatari)
HGVS:: NC_000018.10:g.42073259C>A, NC_000018.10:g.42073259C>G, NC_000018.10:g.42073259C>T, NC_000018.9:g.39653223C>A, NC_000018.9:g.39653223C>G, NC_000018.9:g.39653223C>T

Supplemental Content

dbSNP