RS115388824 CDHR1

Health Risk Chr 10:84213162 snv missense variant
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Associated Conditions
CDHR1-related disorder
Inborn genetic diseases
CDHR1-related disorder
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
0.8%
1kG ALL
0.2%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in CDHR1
rs781781440 rs747425652 rs763399323 rs786205459 rs786205613 rs794726954 rs794727197 rs190906755 rs878853347 rs137876961
Ask Dr. Hemsworth about this variant