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Links from Gene

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A46
(P67S)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
SLC25A46, TMEM232
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
LOC129994343, SLC25A46
Single nucleotide variant
(intron variant)
not provided
GBenign
SLC25A46, TMEM232
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SLC25A46, TMEM232
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SLC25A46
Deletion
Neuropathy, hereditary motor and sensory, type 6B
GPathogenic
SLC25A46
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GUncertain significance
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