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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IGSF10, MED12L
(N2130K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
IGSF10, MED12L
(H2179Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance