| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive | |
| | | Single nucleotide variant (synonymous variant +1 more) | Neural tube defects, folate-sensitive | |
| | C1orf167, MTHFR (L1303del) | Deletion (inframe_deletion +1 more) | Neural tube defects, folate-sensitive | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive | |
| | | Duplication (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive | |
| | | Deletion (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive +1 more | |
| | | Deletion (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive | |
| | | Duplication (3 prime UTR variant +1 more) | Neural tube defects, folate-sensitive | |
Click to view in NCBI Gene