RS869312931 BRAT1

Health Risk Chr 7:2543589
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
Inborn genetic diseases
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
Other Variants in BRAT1
rs730880324 rs1554296088 rs727505363 rs727505364 rs727505365 rs794729222 rs140451075 rs886039312 rs776913277 rs763527391
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