U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSRB3
Single nucleotide variant
(splice acceptor variant)
Autosomal recessive nonsyndromic hearing loss 74
GLikely pathogenic
MSRB3
(C128Y +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 74
GUncertain significance
MSRB3
(V81del +1 more)
Microsatellite
(inframe_deletion)
Autosomal recessive nonsyndromic hearing loss 74
GUncertain significance
MSRB3
(M1R)
Single nucleotide variant
(5 prime UTR variant +2 more)
Autosomal recessive nonsyndromic hearing loss 74
GLikely pathogenic
MSRB3
Single nucleotide variant
(splice acceptor variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MSRB3
Single nucleotide variant
(splice donor variant +1 more)
Autosomal recessive nonsyndromic hearing loss 74
GUncertain significance
MSRB3
(G136R +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 74
GLikely pathogenic
MSRB3
Single nucleotide variant
(splice acceptor variant)
Autosomal recessive nonsyndromic hearing loss 74
GPathogenic
MSRB3
(R19*)
Single nucleotide variant
(nonsense +1 more)
Autosomal recessive nonsyndromic hearing loss 74
GPathogenic
MSRB3
(C89G +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 74
GPathogenic
Format
Items per page
Sort by
Choose Destination