RS139512218 SPRY4

Health Risk Chr 5:142314455 snv missense variant
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Associated Conditions
ClinVar Assertions (1)
NM_001127496.3(SPRY4):c.653C>A (p.Ser218Tyr)
· 6 submitters
Population Frequencies
gnomAD ALL
99.4%
1kG AFR
100%
1kG ALL
99.8%
1kG AMR
0.4%
1kG EAS
100%
1kG EUR
0.8%
1kG SAS
99.9%
Other Variants in SPRY4
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