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Links from MedGen

Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ROR1
(E452D)
Single nucleotide variant
(missense variant)
Hearing loss, autosomal recessive 108
+1 more
GLikely benign
ROR1
(P547S)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ROR1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
ROR1
Single nucleotide variant
(synonymous variant)
Hearing loss, autosomal recessive 108
+1 more
GBenign
ROR1
(T518M)
Single nucleotide variant
(missense variant)
Hearing loss, autosomal recessive 108
+1 more
GBenign
ROR1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
ROR1
(Y910D)
Single nucleotide variant
(missense variant)
Hearing loss, autosomal recessive 108
GUncertain significance
ROR1
(R736T)
Single nucleotide variant
(missense variant)
Hearing loss, autosomal recessive 108
GPathogenic
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