RS117056996 LAMA3

Health Risk Chr 18:23943969 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Laryngo-onycho-cutaneous syndrome
Junctional epidermolysis bullosa gravis of Herlitz
Inborn genetic diseases
Laryngo-onycho-cutaneous syndrome
Junctional epidermolysis bullosa gravis of Herlitz
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in LAMA3
rs2511272040 rs137852757 rs80356679 rs80356678 rs786204732 rs886039412 rs139823161 rs141472847 rs140561492 rs145241852
Ask Dr. Hemsworth about this variant