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Select item 18008491.

rs1800849 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 11:74009120 (GRCh38)
11:73720165 (GRCh37)
Canonical SPDI:: NC_000011.10:74009119:G:A,NC_000011.10:74009119:G:C,NC_000011.10:74009119:G:T
Gene:: UCP3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.217837/19811 (ALFA)
A=0.111111/24 (Qatari)
A=0.153846/12 (PRJEB36033)
A=0.155556/294 (HapMap)
A=0.181918/1165 (1000Genomes_30X)
A=0.186102/932 (1000Genomes)
A=0.189214/50083 (TOPMED)
A=0.210375/438 (HGDP_Stanford)
A=0.235294/40 (GnomAD_exomes)
A=0.237675/916 (ALSPAC)
A=0.239479/239 (GoNL)
A=0.240741/52 (Vietnamese)
A=0.244876/908 (TWINSUK)
A=0.25/10 (GENOME_DK)
A=0.293668/538 (Korea1K)
A=0.298479/2158 (Korea4K)
A=0.3/879 (KOREAN)
A=0.310444/24042 (TOMMO)
A=0.316071/1416 (Estonian)
A=0.321667/193 (NorthernSweden)
A=0.344304/272 (PRJEB37584)
G=0.382353/13 (Siberian)
G=0.425/85 (SGDP_PRJ)
HGVS:: NC_000011.10:g.74009120G>A, NC_000011.10:g.74009120G>C, NC_000011.10:g.74009120G>T, NC_000011.9:g.73720165G>A, NC_000011.9:g.73720165G>C, NC_000011.9:g.73720165G>T, NG_011515.1:g.5118C>T, NG_011515.1:g.5118C>G, NG_011515.1:g.5118C>A, NG_123516.1:g.527G>A, NG_123516.1:g.527G>C, NG_123516.1:g.527G>T, NM_003356.3:c.-238C>T, NM_003356.3:c.-238C>G, NM_003356.3:c.-238C>A, NM_022803.2:c.-238C>T, NM_022803.2:c.-238C>G, NM_022803.2:c.-238C>A

dbSNP