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Select item 42478881.

rs4247888 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 4:49540061 (GRCh38)
4:49542078 (GRCh37)
Canonical SPDI:: NC_000004.12:49540060:A:C,NC_000004.12:49540060:A:G,NC_000004.12:49540060:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GENOME_DK)
A=0.00158/112 (TOMMO)
A=0.00186/3 (Korea1K)
A=0.00286/8 (KOREAN)
A=0.00568/3 (SGDP_PRJ)
A=0.00926/2 (Qatari)
HGVS:: NC_000004.12:g.49540061A>C, NC_000004.12:g.49540061A>G, NC_000004.12:g.49540061A>T, NC_000004.11:g.49542078A>C, NC_000004.11:g.49542078A>G, NC_000004.11:g.49542078A>T

Supplemental Content

dbSNP