607093.G.1

Country

Lebanon

Subject Variants

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_005957.4:c.665C>T	79	0.19
NM_005957.4:c.1286A>C	201	0.49

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Remarks

205 healthy Lebanese controls. 63 heterozygous for the c.665C>T SNP, and 103 heterozygous for the c.1286A>C SNP. Highest prevalence of the c.1286A>C SNP observed among all populations studied so far

References

Sabbagh et al. 2008