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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HOXA1
(N269S)
Single nucleotide variant
(missense variant +1 more)
Human HOXA1 syndromes
GUncertain significance
HOXA1
(D51H)
Single nucleotide variant
(missense variant)
Intellectual disability
GLikely benign
HOXA1, LOC113748384
Single nucleotide variant
(5 prime UTR variant)
Human HOXA1 syndromes
GUncertain significance
HOXA1
(H72P)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
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