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Links from MedGen

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNAH2
(R1533C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
DNAH2
Single nucleotide variant
(splice donor variant)
Spermatogenic failure 45
GLikely pathogenic
DNAH2
(K1567N)
Single nucleotide variant
(missense variant)
Spermatogenic failure 45
GUncertain significance
DNAH2
(R3882*)
Single nucleotide variant
(nonsense)
Spermatogenic failure 45
GPathogenic
DNAH2
(R2755W)
Single nucleotide variant
(missense variant)
Spermatogenic failure 45
GUncertain significance
DNAH2
(S3835P)
Single nucleotide variant
(missense variant)
Spermatogenic failure 45
GPathogenic
DNAH2
(S2320R)
Single nucleotide variant
(missense variant)
Spermatogenic failure 45
GPathogenic
DNAH2
(R3834*)
Single nucleotide variant
(nonsense)
Spermatogenic failure 45
GPathogenic
DNAH2
(R1924C)
Single nucleotide variant
(missense variant)
Spermatogenic failure 45
GPathogenic
DNAH2
(R3100W)
Single nucleotide variant
(missense variant)
Spermatogenic failure 45
GPathogenic
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