RS137853907 PROM1

Health Risk Chr 4:16000516 snv stop gained
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What This Variant Does
"CLNSIG=5
Associated Conditions
Retinal dystrophy
Cone-rod dystrophy 12
PROM1-related disorder
Autosomal recessive retinitis pigmentosa
Retinal dystrophy
Cone-rod dystrophy 12
PROM1-related disorder
Autosomal recessive retinitis pigmentosa
Population Frequencies
gnomAD ALL
0%
Other Variants in PROM1
rs886037612 rs137853005 rs137853006 rs149028760 rs113895168 rs796051882 rs140872693 rs201559220 rs200290535 rs200620291
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