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Select item 15486551.

rs1548655 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: X:7882676 (GRCh38)
X:7850717 (GRCh37)
Canonical SPDI:: NC_000023.11:7882675:C:A,NC_000023.11:7882675:C:G,NC_000023.11:7882675:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.178608/40618 (ALFA)
T=0./0 (KOREAN)
C=0.1/2 (Siberian)
A=0.1/4 (GENOME_DK)
A=0.105263/4 (PRJEB36033)
C=0.149254/40 (SGDP_PRJ)
A=0.171686/496 (ALSPAC)
A=0.175926/19 (Qatari)
A=0.178533/662 (TWINSUK)
A=0.298967/32240 (GnomAD_genomes)
A=0.33486/88634 (TOPMED)
A=0.357692/744 (HGDP_Stanford)
A=0.404912/643 (HapMap)
A=0.424106/1601 (1000Genomes)
A=0.430593/2069 (1000Genomes_30X)
C=0.446809/21 (Vietnamese)
C=0.482421/2511 (Korea4K)
C=0.490955/32460 (TOMMO)
HGVS:: NC_000023.11:g.7882676C>A, NC_000023.11:g.7882676C>G, NC_000023.11:g.7882676C>T, NC_000023.10:g.7850717C>A, NC_000023.10:g.7850717C>G, NC_000023.10:g.7850717C>T

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