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Links from MedGen

Items: 38

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MGP
(E21V +1 more)
Single nucleotide variant
(missense variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
MGP
(M26T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
+1 more
GBenign/Likely benign
MGP
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MGP
Single nucleotide variant
Keutel syndrome
GUncertain significance
MGP
Single nucleotide variant
Keutel syndrome
GUncertain significance
MGP
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GBenign
MGP
(V16I)
Single nucleotide variant
(missense variant)
Keutel syndrome
GUncertain significance
MGP
Deletion
(intron variant)
not provided
+1 more
GBenign/Likely benign
MGP
Duplication
(intron variant)
MGP-related disorder
+2 more
GBenign
MGP
Single nucleotide variant
(synonymous variant)
Keutel syndrome
+1 more
GConflicting classifications of pathogenicity
MGP
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
MGP
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MGP
Single nucleotide variant
(synonymous variant)
Keutel syndrome
GUncertain significance
MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GLikely benign
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Duplication
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
LOC126861465, MGP
Deletion
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GUncertain significance
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GLikely benign
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
LOC126861465, MGP
Single nucleotide variant
(3 prime UTR variant)
Keutel syndrome
GBenign
MGP
(K53E +1 more)
Single nucleotide variant
(missense variant)
Keutel syndrome
+2 more
GBenign/Likely benign
MGP
(T127A +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
MGP
(N39H +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
MGP
(A8V)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign
MGP
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic/Likely pathogenic
MGP
(Y29* +1 more)
Single nucleotide variant
(nonsense)
Keutel syndrome
GPathogenic
MGP
Single nucleotide variant
(splice acceptor variant)
Keutel syndrome
GPathogenic
MGP
Deletion
(nonsense)
Keutel syndrome
GPathogenic
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