| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | LOC126859646, VARS2 (L457P +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | LOC126859646, VARS2 (R468C +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | LOC126859646, VARS2 (M629T +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126859646, VARS2 (T667A +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (F502Y +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | VARS2-related condition +1 more | |
| | LOC126859646, VARS2 (R657W +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (R670G +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (G675R +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (Q539R +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | LOC126859646, VARS2 (V680L +2 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126859646, VARS2 (I557T +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Microsatellite (intron variant) | not provided | |
| | LOC126859646, VARS2 (K563R +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Combined oxidative phosphorylation defect type 20 +2 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | LOC126859646, VARS2 (A759V +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (C602G +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (R754C +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (R754H +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126859646, VARS2 (V765M +2 more) | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | LOC126859646, VARS2 (R785C +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (R645H +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126859646, VARS2 (E822G +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | LOC126859646, VARS2 (C653Y +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126859646, VARS2 (R825W +2 more) | Single nucleotide variant (missense variant) | not provided | |