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Select item 617341541.

rs61734154 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:78972335 (GRCh38)
17:76968417 (GRCh37)
Canonical SPDI:: NC_000017.11:78972334:A:G
Gene:: LGALS3BP (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.0100143/658 (ALFA)
G=0.0002595/1 (ALSPAC)
G=0.0002697/1 (TWINSUK)
G=0.0020877/2924 (GnomAD_exomes)
G=0.0067594/810 (ExAC)
G=0.0220023/3283 (GnomAD_genomes)
G=0.0232201/302 (GoESP)
G=0.0232667/149 (1000Genomes_30X)
G=0.0233626/117 (1000Genomes)
G=0.0242057/6407 (TOPMED)
G=0.0277778/6 (Qatari)
A=0.4583333/11 (SGDP_PRJ)
HGVS:: NC_000017.11:g.78972335A>G, NC_000017.10:g.76968417A>G, NM_005567.4:c.999T>C, NM_005567.3:c.999T>C

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