ClinVar Miner

List of variants reported as uncertain significance for Alstrom syndrome by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378454.1(ALMS1):c.1451G>T (p.Gly484Val)	rs374663067
NM_001378454.1(ALMS1):c.4792T>A (p.Ser1598Thr)	rs2466102790
NM_001378454.1(ALMS1):c.5056G>A (p.Glu1686Lys)	rs1553403999

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