| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Duplication (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Duplication (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Insertion (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Deletion (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | AMN, LOC130056554 (A372fs) | Duplication (frameshift variant) | Imerslund-Grasbeck syndrome | |
| | | Deletion (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Duplication (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | AMN, LOC130056554 (R323fs) | Deletion (frameshift variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Deletion (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome | |
| | | Duplication (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome | |
| | | Indel (missense variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome | |
| | | Duplication (frameshift variant) | Imerslund-Grasbeck syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome type 2 +1 more | |
| | | Duplication (inframe_insertion) | Imerslund-Grasbeck syndrome type 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Imerslund-Grasbeck syndrome | |
| | AMN, LOC130056554 (E317fs) | Deletion (frameshift variant) | Imerslund-Grasbeck syndrome | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome type 2 +1 more | |
| | | Indel (frameshift variant) | Imerslund-Grasbeck syndrome type 2 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Imerslund-Grasbeck syndrome type 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome | |
| | | Deletion (splice acceptor variant) | Imerslund-Grasbeck syndrome type 2 | |
| | AMN, LOC130056554 (E348fs) | Indel (frameshift variant) | Imerslund-Grasbeck syndrome type 2 | |
| | | Single nucleotide variant (missense variant) | Imerslund-Grasbeck syndrome | |