RS121917882 SLC19A3

Health Risk Chr 2:227702250 snv missense variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
Biotin-responsive basal ganglia disease
Inborn genetic diseases
Biotin-responsive basal ganglia disease
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
Other Variants in SLC19A3
rs121917884 rs137852957 rs137852958 rs713993048 rs786205213 rs188532608 rs756676536 rs863224204 rs563607795 rs142166552
Ask Dr. Hemsworth about this variant