U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXH1
Single nucleotide variant
(3 prime UTR variant)
Holoprosencephaly sequence
+2 more
GBenign
FOXH1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
FOXH1
(D328E)
Single nucleotide variant
(missense variant)
Holoprosencephaly sequence
+1 more
GBenign/Likely benign
FOXH1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
FOXH1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
FOXH1
(G177R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FOXH1
(F167L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
FOXH1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
FOXH1
(T125S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
FOXH1
Single nucleotide variant
(synonymous variant)
Holoprosencephaly sequence
+1 more
GBenign
FOXH1
(S113T)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
FOXH1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination