RS119489101 EFEMP2

Health Risk Chr 11:65871354 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Cutis laxa
autosomal recessive
type 1A
type 1B
Cutis laxa
autosomal recessive
type 1A
type 1B
Population Frequencies
gnomAD ALL
0%
Other Variants in EFEMP2
rs119489102 rs193302865 rs193302868 rs193302867 rs193302869 rs193302870 rs193302864 rs193302866 rs397514683 rs572394429
Ask Dr. Hemsworth about this variant