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Links from Gene

Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GFRA4, LOC130065333
(L153P)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
GFRA4, LOC130065334
(S108L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GFRA4, LOC130065334
(P139Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
GFRA4, LOC130065333
(R175G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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