List of variants in gene MYD88 reported as benign for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002468.5(MYD88):c.36C>G (p.Ala12=)	rs79867863	0.00473
NM_002468.5(MYD88):c.80T>C (p.Met27Thr)	rs201871349	0.00372
NM_002468.5(MYD88):c.328+11C>T	rs201931967	0.00064
NM_002468.5(MYD88):c.644+3T>C	rs148149492	0.00043
NM_002468.5(MYD88):c.270C>G (p.Leu90=)	rs143752366	0.00031
NM_002468.5(MYD88):c.604A>C (p.Thr202Pro)	rs191826554	0.00029
NM_002468.5(MYD88):c.261C>T (p.Gly87=)	rs373382593	0.00009
NM_002468.5(MYD88):c.579G>A (p.Val193=)	rs144836346	0.00009

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