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Select item 20741921.

rs2074192 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:15564667 (GRCh38)
X:15582790 (GRCh37)
Canonical SPDI:: NC_000023.11:15564666:C:T
Gene:: ACE2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.430587/24385 (ALFA)
C=0.147059/5 (Siberian)
C=0.176692/47 (SGDP_PRJ)
T=0.324074/35 (Qatari)
T=0.325/13 (GENOME_DK)
T=0.363179/1371 (1000Genomes)
T=0.363371/1746 (1000Genomes_30X)
T=0.37412/425 (Daghestan)
T=0.382979/108 (PharmGKB)
T=0.394125/104321 (TOPMED)
T=0.396341/130 (HapMap)
T=0.402129/43522 (GnomAD_genomes)
C=0.4375/21 (Vietnamese)
T=0.450642/2351 (Korea4K)
T=0.452238/29921 (TOMMO)
T=0.454577/1331 (KOREAN)
T=0.456311/1692 (TWINSUK)
T=0.465905/1346 (ALSPAC)
HGVS:: NC_000023.11:g.15564667C>T, NC_000023.10:g.15582790C>T, NG_012575.3:g.47544G>A, NG_012575.2:g.42492G>A

dbSNP