List of variants in gene TMEM67 reported as benign by PreventionGenetics, part of Exact Sciences

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_153704.6(TMEM67):c.1066-3C>T	rs3097427	0.65135
NM_153704.6(TMEM67):c.1810A>G (p.Ile604Val)	rs3134031	0.64845
NM_153704.6(TMEM67):c.2892A>C (p.Thr964=)	rs16916221	0.04084
NM_153704.6(TMEM67):c.1518+18T>C	rs73694953	0.01972
NM_001142301.1(TMEM67):c.-200G>C	rs79833026	0.01971
NM_153704.6(TMEM67):c.406+1379G>A	rs60659894	0.01971
NM_153704.6(TMEM67):c.870-29A>G	rs116802062	0.01936
NM_153704.6(TMEM67):c.*19T>C	rs55850117	0.01744
NM_153704.6(TMEM67):c.1288+46C>T	rs73694952	0.01390
NM_153704.6(TMEM67):c.2397T>C (p.Asp799=)	rs117195541	0.01237
NM_153704.6(TMEM67):c.781G>A (p.Asp261Asn)	rs35793208	0.01141
NM_153704.6(TMEM67):c.312+30C>G	rs74712633	0.00588
NM_153704.6(TMEM67):c.870-30C>T	rs115933371	0.00474
NM_153704.6(TMEM67):c.2952A>G (p.Ala984=)	rs115967793	0.00439
NM_153704.6(TMEM67):c.507-19T>C	rs138589757	0.00344

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