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Select item 43571471.

rs4357147 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:154068844 (GRCh38)
6:154389979 (GRCh37)
Canonical SPDI:: NC_000006.12:154068843:A:G
Gene:: OPRM1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.002904/367 (ALFA)
G=0./0 (PRJEB36033)
G=0.003195/2 (Chileans)
G=0.00463/1 (Qatari)
G=0.006238/13 (HGDP_Stanford)
G=0.013402/1999 (GnomAD_genomes)
G=0.014942/3955 (TOPMED)
G=0.014976/75 (1000Genomes)
G=0.015771/101 (1000Genomes_30X)
G=0.033997/41 (HapMap)
A=0.5/4 (SGDP_PRJ)
HGVS:: NC_000006.12:g.154068844A>G, NC_000006.11:g.154389979A>G, NG_021208.2:g.63344A>G

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