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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STIM1
Single nucleotide variant
(intron variant)
STIM1-related disorder
+3 more
GConflicting classifications of pathogenicity
STIM1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+4 more
GBenign/Likely benign
STIM1
(S524F +9 more)
Single nucleotide variant
(missense variant +2 more)
STIM1-related disorder
+5 more
GConflicting classifications of pathogenicity
LOC124418421, STIM1
Single nucleotide variant
(synonymous variant +2 more)
STIM1-related disorder
+4 more
GLikely benign
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