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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCM
(V1857M +1 more)
Single nucleotide variant
(missense variant)
Spermatogenic failure 28
+4 more
GUncertain significance
FANCM
Deletion
(genic downstream transcript variant +1 more)
Fanconi anemia, complementation group M
GUncertain significance
FANCM
(S724* +1 more)
Single nucleotide variant
(nonsense)
Fanconi anemia, complementation group M
GUncertain significance
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