List of variants in gene PNPLA6 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001166114.2(PNPLA6):c.2094G>A (p.Pro698=)	rs8107538	0.26133
NM_001166114.2(PNPLA6):c.1207G>C (p.Ala403Pro)	rs17854645	0.16605
NM_001166114.2(PNPLA6):c.765C>T (p.Asn255=)	rs591040	0.07584
NM_001166114.2(PNPLA6):c.1457C>T (p.Pro486Leu)	rs145191932	0.00466
NM_001166114.2(PNPLA6):c.414-18C>T	rs149630061	0.00421
NM_001166114.2(PNPLA6):c.1005+14G>A	rs190321280	0.00371
NM_006702.5(PNPLA6):c.-43+3G>A	rs185247203	0.00274
NM_001166114.2(PNPLA6):c.3234C>T (p.Asn1078=)	rs148831568	0.00174
NM_001166114.2(PNPLA6):c.2359G>A (p.Val787Met)	rs145988230	0.00160
NM_001166114.2(PNPLA6):c.2385C>T (p.His795=)	rs143914980	0.00136
NM_001166114.2(PNPLA6):c.1109C>T (p.Pro370Leu)	rs200897068	0.00128
NM_001166114.2(PNPLA6):c.315+13C>T	rs200676307	0.00094
NM_001166114.2(PNPLA6):c.1530+11G>A	rs184998637	0.00087
NM_001166114.2(PNPLA6):c.3912C>T (p.Asp1304=)	rs149871062	0.00087
NM_001166114.2(PNPLA6):c.3699+17G>A	rs141831508	0.00026
NM_001166114.2(PNPLA6):c.225A>G (p.Arg75=)	rs553088930	0.00023
NM_001166114.2(PNPLA6):c.2818-4C>T	rs533705093	0.00019
NM_001166114.2(PNPLA6):c.796-11C>T	rs758381371	0.00010
NM_001166114.2(PNPLA6):c.3450G>A (p.Gly1150=)	rs367675784	0.00007
NM_001166114.2(PNPLA6):c.3606A>G (p.Leu1202=)	rs200234059	0.00005
NM_001166114.2(PNPLA6):c.1626C>T (p.Phe542=)	rs778970098	0.00004
NM_001166114.2(PNPLA6):c.3280+12C>T	rs201782128	0.00004
NM_001166114.2(PNPLA6):c.2185-15C>T	rs780822241	0.00003
NM_001166114.2(PNPLA6):c.232+14G>A	rs199727584	0.00003
NM_001166114.2(PNPLA6):c.3105G>A (p.Ser1035=)	rs779667737	0.00002
NM_001166114.2(PNPLA6):c.2523C>T (p.Ile841=)	rs375484169	0.00001
NM_001166114.2(PNPLA6):c.3281-7C>T	rs762489747	0.00001
NM_001166114.2(PNPLA6):c.946C>A (p.Arg316=)	rs1352475389	0.00001

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