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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC125371439, TSHZ1
(S402L +1 more)
Single nucleotide variant
(missense variant)
TSHZ1-related condition
GUncertain significance
LOC125371439, TSHZ1
(V464E +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LOC125371439, TSHZ1
Single nucleotide variant
(synonymous variant)
TSHZ1-related condition
GBenign
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