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Select item 25697501.

rs2569750 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 19:50838979 (GRCh38)
19:51342235 (GRCh37)
Canonical SPDI:: NC_000019.10:50838978:A:C,NC_000019.10:50838978:A:G
Gene:: LOC105372441 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.05884/698 (ALFA)
G=0.00373/61 (TOMMO)
G=0.01178/59 (1000Genomes)
G=0.02628/877 (GnomAD)
G=0.02778/6 (Qatari)
G=0.08252/237 (KOREAN)
A=0.5/9 (SGDP_PRJ)
HGVS:: NC_000019.10:g.50838979A>C, NC_000019.10:g.50838979A>G, NC_000019.9:g.51342235A>C, NC_000019.9:g.51342235A>G

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