RS139526942 NAGPA

Health Risk Chr 16:5028123 snv missense variant
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What This Variant Does
"rs139526942, also known as c.982C&gt
Associated Conditions
Stuttering
familial persistent
2
Stuttering
familial persistent
2
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
99.9%
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