RS13073139 BTD

Health Risk Chr 3:15644366 snv missense variant
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What This Variant Does
"[OMIM:BIOTINIDASE DEFICIENCY]
Associated Conditions
Biotinidase deficiency
Inborn genetic diseases
Biotinidase deficiency
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0.1%
Other Variants in BTD
rs80338684 rs104893688 rs80338686 rs119103232 rs13078881 rs28934601 rs80338685 rs104893692 rs104893686 rs104893687
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