NG_007462.1:g.3959T>C

HGVS Expressions

  • NG_007462.1:g.3959T>C

Associated Genes

Tumor Necrosis Factor
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Genomic Location

chr6:31574531

CTGA Clinical Significance

Risk factor

Variant Type

Substitution

dbSNP

1799964

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
614389.G.1.1Bahrain880.17Risk factorPregnancy Loss, Recurrent, Susceptibility to, 1Finan et al. 2010 36 heterozygotes and 16 homozygotes in a...
614389.G.1.2Bahrain290.06Risk factorFinan et al. 2010 Study of 248 controls
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