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Select item 115446121.

rs11544612 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:8364208 (GRCh38)
19:8429092 (GRCh37)
Canonical SPDI:: NC_000019.10:8364207:G:A
Gene:: ANGPTL4 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.010636/271 (ALFA)
A=0.002484/2234 (GnomAD_exomes)
A=0.009259/2 (Qatari)
A=0.023962/120 (1000Genomes)
A=0.023978/3579 (GnomAD_genomes)
A=0.024984/160 (1000Genomes_30X)
A=0.027326/7233 (TOPMED)
G=0.409091/9 (SGDP_PRJ)
HGVS:: NC_000019.10:g.8364208G>A, NC_000019.9:g.8429092G>A, NG_012169.1:g.5082G>A, NM_139314.3:c.-114G>A, NM_139314.2:c.-114G>A, NM_139314.1:c.-114G>A, NM_001039667.3:c.-114G>A, NM_001039667.2:c.-114G>A, NM_001039667.1:c.-114G>A, NR_104213.2:n.54G>A, NR_104213.1:n.82G>A, XM_005272484.4:c.-114G>A, XM_005272484.3:c.-114G>A, XM_005272484.2:c.-114G>A, XM_005272484.1:c.-114G>A, XM_005272485.4:c.-114G>A, XM_005272485.3:c.-114G>A, XM_005272485.2:c.-114G>A, XM_005272485.1:c.-114G>A, NM_016109.2:c.-114G>A, NM_016109.1:c.-114G>A

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11544612[uid] (1)
SNP
3737085[uid] (1)
SNP
627099[uid] (1)
SNP
135551[uid] (1)
SNP
Homo sapiens RAB3 GTPase activating protein subunit 1 (catalytic) (RAB3GAP1), mR...
Homo sapiens RAB3 GTPase activating protein subunit 1 (catalytic) (RAB3GAP1), mRNA
gi|55743117|ref|NM_012233.1|

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