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Select item 114663451.

rs11466345 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 19:41337556 (GRCh38)
19:41843461 (GRCh37)
Canonical SPDI:: NC_000019.10:41337555:T:A,NC_000019.10:41337555:T:C,NC_000019.10:41337555:T:G
Gene:: TGFB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.099865/3406 (ALFA)
C=0.075/3 (GENOME_DK)
C=0.077154/77 (GoNL)
C=0.079827/296 (TWINSUK)
C=0.082252/317 (ALSPAC)
C=0.086667/52 (NorthernSweden)
C=0.118902/39 (HapMap)
C=0.120722/17990 (GnomAD_genomes)
C=0.126325/33437 (TOPMED)
C=0.143897/11249 (PAGE_STUDY)
C=0.148148/32 (Qatari)
C=0.153186/981 (1000Genomes_30X)
C=0.153954/771 (1000Genomes)
C=0.158295/12259 (TOMMO)
C=0.243572/1762 (Korea4K)
C=0.25256/740 (KOREAN)
C=0.262402/201 (PRJEB37584)
C=0.310185/67 (Vietnamese)
T=0.38587/71 (SGDP_PRJ)
T=0.5/9 (Siberian)
HGVS:: NC_000019.10:g.41337556T>A, NC_000019.10:g.41337556T>C, NC_000019.10:g.41337556T>G, NC_000019.9:g.41843461T>A, NC_000019.9:g.41843461T>C, NC_000019.9:g.41843461T>G, NG_013364.1:g.21371A>T, NG_013364.1:g.21371A>G, NG_013364.1:g.21371A>C

dbSNP