RS71785313 APOL1

Health Risk Chr 22:36265995 delins inframe deletion
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What This Variant Does
"The derived allele of indel rs71785313 (p.NYK388K) defines the APOL1 G2 allele. This allele has been...
Associated Conditions
Population Frequencies
gnomAD ALL
0.4%
1kG AFR
87.1%
1kG ALL
96.5%
1kG AMR
0.9%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in APOL1
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