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Links from MedGen

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SEPTIN12
(T256I +1 more)
Single nucleotide variant
(missense variant)
Spermatogenic failure 10
GUncertain significance
SEPTIN12
(D197N +1 more)
Single nucleotide variant
(missense variant)
Spermatogenic failure 10
Grisk factor
SEPTIN12
(T89M)
Single nucleotide variant
(missense variant)
Spermatogenic failure 10
Grisk factor
SEPTIN12
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
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