List of variants in gene PYGM reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_005609.4(PYGM):c.1518+171A>T	rs565688	0.91683
NM_005609.4(PYGM):c.528+74C>A	rs489192	0.80888
NM_005609.4(PYGM):c.999+99T>C	rs625172	0.76387
NM_005609.4(PYGM):c.1403+49C>A	rs2959652	0.73328
NM_005609.4(PYGM):c.660+35G>A	rs589691	0.68983
NM_005609.4(PYGM):c.529-82G>A	rs490980	0.68643
NM_005609.4(PYGM):c.243+48A>G	rs477549	0.20640
NM_005609.3(PYGM):c.-381T>C	rs483962	0.20383
NM_005609.4(PYGM):c.1969+293A>G	rs506354	0.13976
NM_005609.4(PYGM):c.1969+286G>C	rs592546	0.13973
NM_005609.4(PYGM):c.1969+272T>C	rs592521	0.13373
NM_005609.4(PYGM):c.1969+277G>A	rs2071320	0.13369
NM_005609.4(PYGM):c.1969+280A>G	rs592532	0.13366
NM_005609.4(PYGM):c.2313-47T>C	rs569602	0.10954
NM_005609.4(PYGM):c.1519-279G>C	rs7126110	0.10682
NM_005609.4(PYGM):c.1827+7A>G	rs532747	0.10554
NM_005609.4(PYGM):c.661-464G>T	rs547066	0.09765
NM_005609.4(PYGM):c.1768+51C>T	rs686171	0.08974
NM_005609.4(PYGM):c.1494C>T (p.Pro498=)	rs11231865	0.03355
NM_005609.4(PYGM):c.425-22C>T	rs61884454	0.02517
NM_005609.4(PYGM):c.1184C>T (p.Thr395Met)	rs71581787	0.01778
NM_005609.4(PYGM):c.1569C>G (p.Leu523=)	rs114138772	0.01143
NM_005609.4(PYGM):c.645G>A (p.Lys215=)	rs116315896	0.00530
NM_005609.4(PYGM):c.2009C>T (p.Ala670Val)	rs113806080	0.00446
NM_005609.4(PYGM):c.182G>A (p.Arg61His)	rs145514333	0.00058
NM_005609.4(PYGM):c.1692C>T (p.Phe564=)	rs116812032	0.00041
NM_005609.4(PYGM):c.-76A>G	rs139467558	0.00030
NM_005609.4(PYGM):c.1240C>G (p.Arg414Gly)	rs11231866
NM_005609.4(PYGM):c.1969+266_1969+267insAC	rs58190568

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