RS138168899 LAMA3

Health Risk Chr 18:23881942 snv missense variant
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.4%
1kG ALL
0.2%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in LAMA3
rs2511272040 rs137852757 rs80356679 rs80356678 rs786204732 rs886039412 rs139823161 rs141472847 rs140561492 rs145241852
Ask Dr. Hemsworth about this variant