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rs1060505041(C;T)

From SNPedia
Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination
Is agenotype
ofrs1060505041
GeneNACC1
Chromosome19
Position13,136,099
mentionedby
Magnitude8
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 8 Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination

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