NM_000129.4:c.103G>T

HGVS Expressions

  • NG_008107.1:g.7130G>T
  • NM_000129.4:c.103G>T
  • NP_000120.2:p.Val35Leu
  • NC_000006.12:g.6318562C>A

Associated Genes

Factor XIII, A1 Subunit
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Clinical Significance

Benign,Protective,Uncertain Significance

Variant Type

Substitution

dbSNP

5985

Clinvar

16532

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
134570.G.1Lebanon304BenignMahfouz et al, 2008 Group of 152 healthy Lebanese individual...
134570.G.2Lebanon46BenignMahfouz et al, 2008 Group of 46 healthy Lebanese individuals...
134570.G.3Lebanon14BenignMahfouz et al, 2008 Group of 7 healthy Lebanese individuals ...
601367.23Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with arterial lesion
601367.29Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with small vessel lesion
601367.3Lebanon2Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.30Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with small vessel lesion
601367.5Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
601367.6Lebanon1Uncertain SignificanceStroke, IschemicAraji et al. 2014 Stroke patient with spinal lesion
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