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Select item 255311.

rs25531 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 17:30237328 (GRCh38)
17:28564346 (GRCh37)
Canonical SPDI:: NC_000017.11:30237327:T:C,NC_000017.11:30237327:T:G
Gene:: SLC6A4 (Varview), LOC105371720 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.026408/315 (ALFA)
C=0.025/1 (GENOME_DK)
C=0.045373/601 (TOMMO)
C=0.046296/10 (Qatari)
C=0.070039/36 (NorthernSweden)
C=0.097222/133 (Korea1K)
C=0.098227/266 (KOREAN)
C=0.119181/31546 (TOPMED)
C=0.13758/689 (1000Genomes)
C=0.181502/5432 (GnomAD)
T=0.441667/53 (SGDP_PRJ)
T=0.5/2 (Siberian)
HGVS:: NC_000017.11:g.30237328T>C, NC_000017.11:g.30237328T>G, NC_000017.10:g.28564346T>C, NC_000017.10:g.28564346T>G, NG_011747.2:g.3609A>G, NG_011747.2:g.3609A>C, NG_055470.1:g.1948T>C, NG_055470.1:g.1948T>G