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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CD70, LOC130063317
(P25T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CD70, LOC130063317
(S9L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CD70, LOC130063316
Single nucleotide variant
(intron variant)
CD70-related disorder
GLikely benign
CD70, LOC130063317
Single nucleotide variant
(5 prime UTR variant)
not specified
GBenign
CD70, LOC130063317
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
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