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Select item 22417661.

rs2241766 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 3:186853103 (GRCh38)
3:186570892 (GRCh37)
Canonical SPDI:: NC_000003.12:186853102:T:A,NC_000003.12:186853102:T:C,NC_000003.12:186853102:T:G
Gene:: ADIPOQ (Varview), ADIPOQ-AS1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.102999/8504 (ALFA)
G=0.048214/216 (Estonian)
G=0.075/45 (NorthernSweden)
G=0.088816/27 (FINRISK)
G=0.092496/1203 (GoESP)
G=0.10521/105 (GoNL)
G=0.114798/30386 (TOPMED)
G=0.125/5 (GENOME_DK)
G=0.125843/485 (ALSPAC)
G=0.127832/474 (TWINSUK)
G=0.128913/15641 (ExAC)
G=0.146627/939 (1000Genomes_30X)
G=0.151358/758 (1000Genomes)
G=0.185185/40 (Qatari)
G=0.207865/111 (MGP)
G=0.285666/837 (KOREAN)
G=0.297095/2148 (Korea4K)
G=0.30165/23361 (TOMMO)
G=0.302402/554 (Korea1K)
G=0.324104/199 (Vietnamese)
T=0.416667/5 (Siberian)
T=0.457895/87 (SGDP_PRJ)
HGVS:: NC_000003.12:g.186853103T>A, NC_000003.12:g.186853103T>C, NC_000003.12:g.186853103T>G, NC_000003.11:g.186570892T>A, NC_000003.11:g.186570892T>C, NC_000003.11:g.186570892T>G, NG_021140.1:g.15430T>A, NG_021140.1:g.15430T>C, NG_021140.1:g.15430T>G, NM_004797.4:c.45T>A, NM_004797.4:c.45T>C, NM_004797.4:c.45T>G, NM_004797.3:c.45T>A, NM_004797.3:c.45T>C, NM_004797.3:c.45T>G, NM_001177800.2:c.45T>A, NM_001177800.2:c.45T>C, NM_001177800.2:c.45T>G, NM_001177800.1:c.45T>A, NM_001177800.1:c.45T>C, NM_001177800.1:c.45T>G, NG_044949.1:g.13194T>A, NG_044949.1:g.13194T>C, NG_044949.1:g.13194T>G, NR_046662.2:n.2355A>T, NR_046662.2:n.2355A>G, NR_046662.2:n.2355A>C, NR_046662.1:n.2226A>T, NR_046662.1:n.2226A>G, NR_046662.1:n.2226A>C

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