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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
P2RX2
Single nucleotide variant
(synonymous variant +1 more)
Autosomal dominant nonsyndromic hearing loss 41
+2 more
GBenign
P2RX2
(Q164R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign/Likely benign
P2RX2
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
P2RX2
Single nucleotide variant
(synonymous variant)
P2RX2-related condition
+2 more
GBenign
P2RX2
(K236E +4 more)
Single nucleotide variant
(missense variant)
P2RX2-related condition
+2 more
GLikely benign
P2RX2
(T244M +4 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
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