Related gene-specific medical variations for Gene (Select 8301) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3337454	NM_007166.4(PICALM):c.119A>G (p.Lys40Arg)	LOC126861284, PICALM (K40R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2239633	NM_007166.4(PICALM):c.73A>G (p.Thr25Ala)	LOC126861284, PICALM (T25A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1232582	NM_001206947.2(PICALM):c.-24+314A>G	LOC126861284, PICALM	Single nucleotide variant (intron variant)	not provided	GBenign

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