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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129936987, LRIG1
(N111S +5 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
LOC129936987, LRIG1
(N106S +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129936987, LRIG1
(S190Y +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129936987, LRIG1
(N111I +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129936987, LRIG1
Single nucleotide variant
(synonymous variant)
LRIG1-related disorder
+1 more
GBenign
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