RS1407995 DCT

Health Risk Chr 13:94443758 snv intron variant
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Associated Conditions
Population Frequencies
gnomAD ALL
74.6%
1kG AFR
20.3%
1kG ALL
36.8%
1kG AMR
57.6%
1kG EAS
26.3%
1kG EUR
80.8%
1kG SAS
65%
Other Variants in DCT
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