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Links from MedGen

Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
QRICH2
(V1436M)
Single nucleotide variant
(missense variant +1 more)
Spermatogenic failure 35
GUncertain significance
QRICH2
Single nucleotide variant
(intron variant)
Spermatogenic failure 35
GBenign
QRICH2
Single nucleotide variant
(intron variant)
Spermatogenic failure 35
GBenign
QRICH2
Single nucleotide variant
(synonymous variant +1 more)
Spermatogenic failure 35
+1 more
GBenign
QRICH2
(Y1538* +1 more)
Single nucleotide variant
(nonsense +1 more)
Spermatogenic failure 35
GPathogenic
QRICH2
(Y1167* +1 more)
Single nucleotide variant
(nonsense +1 more)
Spermatogenic failure 35
GPathogenic
QRICH2
(R1013* +1 more)
Single nucleotide variant
(nonsense)
Spermatogenic failure 35
GPathogenic
QRICH2
(W64* +1 more)
Single nucleotide variant
(nonsense +1 more)
Spermatogenic failure 35
GPathogenic
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