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Select item 30937371.

rs3093737 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 13:108215135 (GRCh38)
13:108867483 (GRCh37)
Canonical SPDI:: NC_000013.11:108215134:G:C,NC_000013.11:108215134:G:T
Gene:: LIG4 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.032327/518 (ALFA)
C=0.077275/3480 (GnomAD_genomes)
C=0.096625/647 (Korea4K)
C=0.101619/6152 (TOMMO)
C=0.102091/166 (Korea1K)
C=0.110868/710 (1000Genomes_30X)
C=0.112252/29712 (TOPMED)
C=0.116214/582 (1000Genomes)
C=0.125377/333 (KOREAN)
C=0.12963/28 (Qatari)
C=0.131344/10336 (PAGE_STUDY)
G=0.456897/53 (SGDP_PRJ)
G=0.5/7 (Siberian)
HGVS:: NC_000013.11:g.108215135G>C, NC_000013.11:g.108215135G>T, NC_000013.10:g.108867483G>C, NC_000013.10:g.108867483G>T, NG_007396.1:g.5400C>G, NG_007396.1:g.5400C>A

dbSNP