List of variants in gene PRKCSH reported as likely benign for autosomal dominant polycystic liver 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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001289104.2(PRKCSH):c.351-5C>T	rs76485217	0.00604
NM_001289104.2(PRKCSH):c.469-10G>A	rs188022793	0.00354
NM_001289104.2(PRKCSH):c.416G>A (p.Arg139His)	rs139991238	0.00137
NM_001289104.2(PRKCSH):c.807C>T (p.Tyr269=)	rs201337319	0.00125
NM_001289104.2(PRKCSH):c.834C>T (p.Asp278=)	rs139969239	0.00077
NM_001289104.2(PRKCSH):c.1092G>A (p.Pro364=)	rs142347308	0.00066
NM_001289104.2(PRKCSH):c.1291G>A (p.Val431Ile)	rs368655107	0.00054
NM_001289104.2(PRKCSH):c.438G>A (p.Glu146=)	rs143369158	0.00053
NM_001289104.2(PRKCSH):c.862G>A (p.Asp288Asn)	rs144616910	0.00026
NM_001289104.2(PRKCSH):c.763-41C>T	rs369509968	0.00025
NM_001289104.2(PRKCSH):c.823G>A (p.Ala275Thr)	rs142339453	0.00023
NM_001289104.2(PRKCSH):c.1392C>T (p.His464=)	rs200928002	0.00013
NM_001289104.2(PRKCSH):c.752C>T (p.Ala251Val)	rs138530475	0.00013
NM_001289104.2(PRKCSH):c.1476C>T (p.Cys492=)	rs770480368	0.00008
NM_001289104.2(PRKCSH):c.1536G>A (p.Glu512=)	rs374970694	0.00008
NM_001289104.2(PRKCSH):c.279C>T (p.Asn93=)	rs777837737	0.00007
NM_001289104.2(PRKCSH):c.1590C>T (p.Asp530=)	rs147203239	0.00006
NM_001289104.2(PRKCSH):c.683+9C>A	rs367735502	0.00006
NM_001289104.2(PRKCSH):c.678C>T (p.Asp226=)	rs539988285	0.00004
NM_001289104.2(PRKCSH):c.850-12C>T	rs201874863	0.00003
NM_001289104.2(PRKCSH):c.753G>A (p.Ala251=)	rs756127892	0.00002
NM_001289104.2(PRKCSH):c.975G>A (p.Glu325=)	rs775357974	0.00002
NM_001289104.2(PRKCSH):c.1005C>T (p.Ser335=)	rs145740877	0.00001
NM_001289104.2(PRKCSH):c.324C>T (p.Ser108=)	rs368596083	0.00001
NM_001289104.2(PRKCSH):c.847G>A (p.Glu283Lys)	rs776575609	0.00001
NM_001289104.2(PRKCSH):c.1338C>T (p.Leu446=)	rs540593191
NM_001289104.2(PRKCSH):c.1569G>T (p.Pro523=)	rs149505716
NM_001289104.2(PRKCSH):c.327C>T (p.Gly109=)	rs766039060
NM_001289104.2(PRKCSH):c.362G>T (p.Arg121Leu)	rs377537927
NM_001289104.2(PRKCSH):c.781A>T (p.Thr261Ser)	rs1156928058

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