| | ARMC2, SESN1 (R350H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (N240S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, ARMC2-AS1 (S195G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, ARMC2-AS1 (R218T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (N259S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (A197V +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (N215S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (N86S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (D81E +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (H196R +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (R109S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ARMC2, SESN1 (I472T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (T373P +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (Y368F +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not specified | |
| | | Single nucleotide variant (synonymous variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (intron variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | ARMC2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (missense variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (missense variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | ARMC2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (missense variant) | ARMC2-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | ARMC2-related disorder | |
| | | Copy number loss | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (D329H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | ARMC2, SESN1 (P281A +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (R80H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (I120T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (A123V +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (G37R +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | ARMC2, SESN1 (Y356C +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | ARMC2, SESN1 (D453G +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | ARMC2-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Copy number loss | Deletion 6q16 q21 | |
| | | Copy number gain | Microcephaly +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Male infertility with teratozoospermia due to single gene mutation +1 more | |
| | ARMC2, ARMC2-AS1 (K263fs +1 more) | Deletion (frameshift variant) | Male infertility with teratozoospermia due to single gene mutation +1 more | |
| | | Deletion (frameshift variant) | Male infertility with teratozoospermia due to single gene mutation +1 more | |
| | | Single nucleotide variant (missense variant) | Male infertility with teratozoospermia due to single gene mutation +1 more | |
| | | Single nucleotide variant (splice donor variant) | Male infertility with teratozoospermia due to single gene mutation +2 more | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |