RS114160429 SGCG

Health Risk Chr 13:23295447 snv missense variant
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Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2C
SGCG-related disorder
Autosomal recessive limb-girdle muscular dystrophy type 2C
SGCG-related disorder
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.6%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in SGCG
rs2137534216 rs104894422 rs762777463 rs104894423 rs786204786 rs763248287 rs144497243 rs797044783 rs797045106 rs875989949
Ask Dr. Hemsworth about this variant