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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130005991, TM7SF2
(T29A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130005991, TM7SF2
(S39W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130005991, TM7SF2
(G40R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130005991, TM7SF2
Variation
(no sequence alteration +1 more)
not provided
GLikely benign
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