RS887971 IL18RAP

Health Risk Chr 2:102424706 snv intron variant
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Associated Conditions
Population Frequencies
1kG AFR
86.1%
1kG ALL
70.1%
1kG AMR
44.5%
1kG EAS
41.7%
1kG EUR
72.7%
1kG SAS
68.2%
Other Variants in IL18RAP
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