RS72653786 ABCC6

Health Risk Chr 16:16178961
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What This Variant Does
"CLNSIG=1"
Associated Conditions
Autosomal recessive inherited pseudoxanthoma elasticum
Arterial calcification
generalized
of infancy
2
Pseudoxanthoma elasticum
forme fruste
ABCC6-related disorder
Optic atrophy
Autosomal recessive inherited pseudoxanthoma elasticum
Arterial calcification
generalized
of infancy
2
Pseudoxanthoma elasticum
Other Variants in ABCC6
rs72653706 rs72664209 rs60791294 rs63750427 rs72664233 rs63750759 rs387906352 rs63750459 rs28939701 rs72653744
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