RS104894423 SGCG

Health Risk Chr 13:23324452
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2C
Autosomal recessive limb-girdle muscular dystrophy
Inborn genetic diseases
Autosomal recessive limb-girdle muscular dystrophy type 2C
Autosomal recessive limb-girdle muscular dystrophy
Inborn genetic diseases
Other Variants in SGCG
rs2137534216 rs104894422 rs762777463 rs786204786 rs763248287 rs144497243 rs797044783 rs797045106 rs875989949 rs140810408
Ask Dr. Hemsworth about this variant