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Select item 75286841.

rs7528684 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:157701026 (GRCh38)
1:157670816 (GRCh37)
Canonical SPDI:: NC_000001.11:157701025:A:C,NC_000001.11:157701025:A:G,NC_000001.11:157701025:A:T
Gene:: FCRL3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.45994/129475 (ALFA)
T=0./0 (KOREAN)
A=0.29064/118 (SGDP_PRJ)
A=0.321596/548 (HapMap)
A=0.357255/28111 (PAGE_STUDY)
G=0.365402/1637 (Estonian)
G=0.375399/235 (Chileans)
G=0.385098/29822 (TOMMO)
G=0.399563/732 (Korea1K)
G=0.400277/2894 (Korea4K)
G=0.402532/318 (PRJEB37584)
G=0.411215/88 (Vietnamese)
A=0.420084/111192 (TOPMED)
A=0.425/17 (Siberian)
A=0.441818/65822 (GnomAD_genomes)
A=0.442067/2831 (1000Genomes_30X)
A=0.444444/24 (PRJEB36033)
G=0.447327/1724 (ALSPAC)
A=0.449281/2250 (1000Genomes)
G=0.45/18 (GENOME_DK)
G=0.453333/272 (NorthernSweden)
A=0.453704/98 (Qatari)
G=0.467098/1732 (TWINSUK)
G=0.46994/469 (GoNL)
HGVS:: NC_000001.11:g.157701026A>C, NC_000001.11:g.157701026A>G, NC_000001.11:g.157701026A>T, NC_000001.10:g.157670816A>C, NC_000001.10:g.157670816A>G, NC_000001.10:g.157670816A>T, NG_023241.1:g.4832T>G, NG_023241.1:g.4832T>C, NG_023241.1:g.4832T>A

dbSNP