List of variants in gene A2ML1 studied for Otitis media

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_144670.6(A2ML1):c.3676_3677del (p.Ala1226fs)	rs144686314	0.03504
NM_144670.6(A2ML1):c.2713-8C>A	rs184386564	0.00216
NM_144670.6(A2ML1):c.2197T>C (p.Phe733Leu)	rs117213221	0.00051
NM_144670.6(A2ML1):c.2189G>A (p.Arg730His)	rs200346409	0.00009
NM_144670.6(A2ML1):c.971-8C>T	rs780868782	0.00006
NM_144670.6(A2ML1):c.2329G>A (p.Gly777Arg)	rs201288888	0.00002
NM_144670.6(A2ML1):c.10C>T (p.Gln4Ter)	rs1409944554
NM_144670.6(A2ML1):c.1308A>C (p.Gln436His)	rs780743143
NM_144670.6(A2ML1):c.164C>T (p.Thr55Ile)	rs999028234
NM_144670.6(A2ML1):c.1683G>C (p.Gln561His)	rs1565476223
NM_144670.6(A2ML1):c.2012T>C (p.Leu671Pro)	rs1465018225
NM_144670.6(A2ML1):c.2228C>T (p.Pro743Leu)	rs1565479896
NM_144670.6(A2ML1):c.2545G>T (p.Asp849Tyr)	rs1408810942
NM_144670.6(A2ML1):c.2971G>C (p.Ala991Pro)	rs1565484901
NM_144670.6(A2ML1):c.3491C>T (p.Ala1164Val)	rs1565487941
NM_144670.6(A2ML1):c.4061+1G>C	rs202067416

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