List of variants reported as likely benign for Alstrom syndrome by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001378454.1(ALMS1):c.3193T>C (p.Ser1065Pro)	rs28730852	0.00579
NM_001378454.1(ALMS1):c.6752A>G (p.Asp2251Gly)	rs28730855	0.00515
NM_001378454.1(ALMS1):c.4988C>T (p.Thr1663Ile)	rs188807564	0.00267
NM_001378454.1(ALMS1):c.8445A>G (p.Ser2815=)	rs137932254	0.00215
NM_001378454.1(ALMS1):c.945T>C (p.Ser315=)	rs183390773	0.00119
NM_001378454.1(ALMS1):c.11223G>A (p.Glu3741=)	rs28730859	0.00061
NM_001378454.1(ALMS1):c.4149A>G (p.Gln1383=)	rs370508895	0.00016
NM_001378454.1(ALMS1):c.9633G>A (p.Lys3211=)	rs373013570	0.00014
NM_001378454.1(ALMS1):c.764+19A>G	rs1035974697	0.00002
NM_001378454.1(ALMS1):c.36GGA[16] (p.Glu26_Glu28dup)	rs55889738
NM_001378454.1(ALMS1):c.764+20T>G

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