List of variants in gene PKD1 reported as likely benign for Autosomal dominant polycystic kidney disease

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.3275T>C (p.Met1092Thr)	rs2549677	0.19794
NM_001009944.3(PKD1):c.11016+42_11016+43del	rs36224524	0.06371
NM_001009944.3(PKD1):c.8898G>C (p.Glu2966Asp)	rs13337123	0.05219
NM_001009944.3(PKD1):c.8644T>A (p.Trp2882Arg)	rs13333553	0.04733
NM_001009944.3(PKD1):c.107C>A (p.Pro36His)	rs560049593	0.01538
NM_001009944.3(PKD1):c.*15G>A	rs77566834	0.01262
NM_001009944.3(PKD1):c.8123C>T (p.Thr2708Met)	rs147350387	0.01193
NM_001009944.3(PKD1):c.5051C>T (p.Ser1684Leu)	rs139520275	0.00926
NM_001009944.3(PKD1):c.6598C>T (p.Arg2200Cys)	rs140869992	0.00811
NM_001009944.3(PKD1):c.10529C>T (p.Thr3510Met)	rs45478794	0.00702
NM_001009944.3(PKD1):c.8440G>A (p.Gly2814Arg)	rs149151043	0.00622
NM_001009944.3(PKD1):c.4264G>A (p.Ala1422Thr)	rs140980374	0.00485
NM_001009944.3(PKD1):c.6488G>A (p.Arg2163Gln)	rs145217118	0.00290
NM_001009944.3(PKD1):c.9499A>T (p.Ile3167Phe)	rs139945204	0.00125
NM_001009944.3(PKD1):c.8111C>T (p.Ala2704Val)	rs200509641	0.00059
NM_001009944.3(PKD1):c.8335G>A (p.Glu2779Lys)	rs200491536	0.00038
NM_001009944.3(PKD1):c.6965C>T (p.Thr2322Met)	rs564570407	0.00026
NM_001009944.3(PKD1):c.3679G>T (p.Ala1227Ser)	rs150710956	0.00022
NM_001009944.3(PKD1):c.*8T>G	rs767068030	0.00017
NM_001009944.3(PKD1):c.1673C>T (p.Thr558Met)	rs781572938	0.00009
NM_001009944.3(PKD1):c.9620C>T (p.Thr3207Met)	rs200214266	0.00006
NM_001009944.3(PKD1):c.1202-10C>T	rs529554291	0.00005
NM_001009944.3(PKD1):c.7222C>T (p.Arg2408Cys)	rs538769374	0.00002
NM_001009944.3(PKD1):c.1643C>T (p.Ala548Val)	rs768613812	0.00001
NM_001009944.3(PKD1):c.12003+13C>T
NM_001009944.3(PKD1):c.3101A>G (p.Asn1034Ser)	rs28681051
NM_001009944.3(PKD1):c.3502C>T (p.Pro1168Ser)	rs146887330
NM_001009944.3(PKD1):c.8207C>G (p.Pro2736Arg)	rs760592410

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