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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861316, MMP8
(A20T)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC126861316, MMP8
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
LOC126861316, MMP8
(T32I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GBenign
MMP8
Single nucleotide variant
Preterm premature rupture of membranes
GPathogenic
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