List of variants reported as benign for Glycogen storage disease, type V by Natera, Inc.

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_005609.4(PYGM):c.1827+7A>G	rs532747	0.10554
NM_005609.4(PYGM):c.1494C>T (p.Pro498=)	rs11231865	0.03592
NM_005609.4(PYGM):c.1184C>T (p.Thr395Met)	rs71581787	0.01778
NM_005609.4(PYGM):c.1569C>G (p.Leu523=)	rs114138772	0.01217
NM_005609.4(PYGM):c.1092+6dup	rs368602234	0.00700
NM_005609.4(PYGM):c.2009C>T (p.Ala670Val)	rs113806080	0.00446
NM_005609.4(PYGM):c.1537A>G (p.Ile513Val)	rs139570786	0.00232
NM_005609.4(PYGM):c.577G>T (p.Ala193Ser)	rs77656150	0.00209
NM_005609.4(PYGM):c.924C>T (p.Ile308=)	rs139726186	0.00175
NM_005609.4(PYGM):c.1957C>G (p.Leu653Val)	rs61736659	0.00065
NM_005609.4(PYGM):c.182G>A (p.Arg61His)	rs145514333	0.00058
NM_005609.4(PYGM):c.1527G>T (p.Gly509=)	rs114730784	0.00023
NM_005609.4(PYGM):c.2290A>G (p.Asn764Asp)	rs190548494	0.00016
NM_005609.4(PYGM):c.1240C>G (p.Arg414Gly)	rs11231866
NM_005609.4(PYGM):c.1339A>C (p.Ile447Leu)	rs568496266
NM_005609.4(PYGM):c.661-5C>G	rs75633423

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