RS113993961 WRN

Health Risk Chr 8:31141680
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What This Variant Does
"rs113993961 is a rare transversion in the WRN gene that results in a frameshift of codons 1078 to 10...
Associated Conditions
Werner syndrome
Werner syndrome
Other Variants in WRN
rs121908446 rs121908447 rs606231162 rs587776621 rs17847577 rs369158322 rs121908448 rs281865157 rs281865160 rs149565907
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