RS727505273 GSDME

Health Risk Chr 7:24706389
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 5
Monogenic hearing loss
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 5
Monogenic hearing loss
Other Variants in GSDME
rs1562687726 rs1562687295 rs138980048 rs373787249 rs140666247 rs146399987 rs727502954 rs757421220 rs148716975 rs200758965
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