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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129997823, LFNG
Microsatellite
(inframe_insertion +1 more)
not provided
GUncertain significance
LFNG
Single nucleotide variant
(synonymous variant +1 more)
Spondylocostal dysostosis 3, autosomal recessive
+1 more
GConflicting classifications of pathogenicity
LFNG
(E143del)
Deletion
(inframe_deletion +1 more)
not provided
GUncertain significance
LFNG
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
LFNG
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LFNG
(D231N +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
LFNG
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LFNG
Single nucleotide variant
(synonymous variant)
LFNG-related condition
+1 more
GConflicting classifications of pathogenicity
LFNG
(V346L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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