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Links from MedGen

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH4
Insertion
(intron variant)
Spermatogenic failure 2
+1 more
GBenign
MSH4
Single nucleotide variant
(synonymous variant)
Spermatogenic failure 2
+1 more
GBenign
MSH4
Single nucleotide variant
(synonymous variant)
Premature ovarian failure 20
+1 more
GBenign
MSH4
Single nucleotide variant
(intron variant)
Premature ovarian failure 20
+1 more
GBenign
MSH4
(A97T)
Single nucleotide variant
(missense variant)
Premature ovarian failure 20
+1 more
GBenign
MSH4
(D727fs)
Deletion
(frameshift variant)
Spermatogenic failure 2
GPathogenic
MSH4
(W650*)
Single nucleotide variant
(nonsense)
Spermatogenic failure 2
GPathogenic
MSH4
(V269fs)
Deletion
(frameshift variant)
Spermatogenic failure 2
GPathogenic
MSH4
Single nucleotide variant
(nonsense)
Spermatogenic failure 2
GPathogenic
MSH4
(K741fs)
Deletion
(frameshift variant)
Genetic non-acquired premature ovarian failure
+1 more
GPathogenic
MSH4
(S733*)
Single nucleotide variant
(nonsense)
Non-obstructive azoospermia
GLikely pathogenic
MSH4
(S754L)
Single nucleotide variant
(missense variant)
Oligospermia
+2 more
GPathogenic/Likely pathogenic
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