RS767263985 SLC52A3

Health Risk Chr 20:765401
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What This Variant Does
"CLNSIG=5
Associated Conditions
Brown-Vialetto-van Laere syndrome 1
Inborn genetic diseases
Monogenic hearing loss
Brown-Vialetto-van Laere syndrome 1
Brown-Vialetto-van Laere syndrome 1
Inborn genetic diseases
Monogenic hearing loss
Brown-Vialetto-van Laere syndrome 1
Other Variants in SLC52A3
rs794728004 rs267606683 rs267606685 rs267606686 rs267606688 rs754753126 rs752218005 rs778363575 rs778479139 rs199588390
Ask Dr. Hemsworth about this variant