Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000169749 | SCV000221299 | pathogenic | Autosomal recessive nonsyndromic hearing loss 29 | 2012-02-01 | no assertion criteria provided | literature only | |
Genetic Testing Center for Deafness, |
RCV000169749 | SCV000902301 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 29 | 2019-02-26 | no assertion criteria provided | case-control |