List of variants in gene IMPG2 reported as benign by Invitae

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_016247.4(IMPG2):c.3381C>T (p.Leu1127=)	rs348867	0.80304
NM_016247.4(IMPG2):c.2021C>T (p.Thr674Ile)	rs571391	0.64801
NM_016247.4(IMPG2):c.666+10G>A	rs533852	0.39987
NM_016247.4(IMPG2):c.3439C>T (p.Pro1147Ser)	rs111784356	0.02010
NM_016247.4(IMPG2):c.1908T>C (p.Asp636=)	rs35648234	0.02002
NM_016247.4(IMPG2):c.828+17_828+18insC	rs199824990	0.01356
NM_016247.4(IMPG2):c.828+17A>C	rs56910465	0.00333
NM_016247.4(IMPG2):c.1544-20A>C	rs201831318	0.00313
NM_016247.4(IMPG2):c.1893G>A (p.Pro631=)	rs149291477	0.00168
NM_016247.4(IMPG2):c.521A>C (p.Glu174Ala)	rs146938670	0.00121
NM_016247.4(IMPG2):c.335-13C>T	rs201277460	0.00098
NM_016247.4(IMPG2):c.1140G>A (p.Leu380=)	rs192551069	0.00044
NM_016247.4(IMPG2):c.3561C>T (p.Ser1187=)	rs139496326	0.00025
NM_016247.4(IMPG2):c.1382C>G (p.Thr461Arg)	rs201905772	0.00017
NM_016247.4(IMPG2):c.57G>C (p.Leu19=)	rs188916371	0.00013
NM_016247.4(IMPG2):c.123C>G (p.Pro41=)	rs183804037	0.00010
NM_016247.4(IMPG2):c.1227G>A (p.Pro409=)	rs371246481	0.00002
NM_016247.4(IMPG2):c.1239+10del	rs751135558
NM_016247.4(IMPG2):c.1239+17del
NM_016247.4(IMPG2):c.1240-3del	rs762013280
NM_016247.4(IMPG2):c.1240-9del	rs557392173
NM_016247.4(IMPG2):c.1240-9dup	rs557392173
NM_016247.4(IMPG2):c.3634-8del
NM_016247.4(IMPG2):c.534-13dup	rs567795716
NM_016247.4(IMPG2):c.828+20del	rs746039015
NM_016247.4(IMPG2):c.85+11dup

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