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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SERPINB6
(I24T +4 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive nonsyndromic hearing loss 91
GUncertain significance
SERPINB6
(M15I +3 more)
Single nucleotide variant
(missense variant +3 more)
Autosomal recessive nonsyndromic hearing loss 91
GLikely pathogenic
SERPINB6
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
SERPINB6
Single nucleotide variant
(intron variant)
not specified
GLikely benign
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