List of variants in gene ABCC6 reported as benign for not specified

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

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001171.6(ABCC6):c.1338+7C>G	rs9940089	0.75013
NM_001171.6(ABCC6):c.3803G>A (p.Arg1268Gln)	rs2238472	0.22903
NM_001171.6(ABCC6):c.793A>G (p.Arg265Gly)	rs72657698	0.06836
NM_001171.6(ABCC6):c.346-6G>A	rs55778939	0.03265
NM_001171.6(ABCC6):c.3871G>A (p.Ala1291Thr)	rs58694313	0.02791
NM_001171.6(ABCC6):c.2175A>T (p.Val725=)	rs59757815	0.02503
NM_001171.6(ABCC6):c.2224A>G (p.Ile742Val)	rs59593133	0.02501
NM_001171.6(ABCC6):c.2836C>A (p.Leu946Ile)	rs61340537	0.01730
NM_001171.6(ABCC6):c.3190C>T (p.Arg1064Trp)	rs41278174	0.01708
NM_001171.6(ABCC6):c.2171G>A (p.Arg724Lys)	rs58073789	0.01638
NM_001171.6(ABCC6):c.3507-3C>T	rs41278172	0.01517
NM_001171.6(ABCC6):c.1077A>G (p.Ser359=)	rs72664283	0.01355
NM_001171.6(ABCC6):c.4208+9G>A	rs58760581	0.01119
NM_001171.6(ABCC6):c.487G>A (p.Asp163Asn)	rs192110266	0.00934
NM_001171.6(ABCC6):c.3289C>A (p.Leu1097Ile)	rs60707953	0.00849
NM_001171.6(ABCC6):c.2067C>T (p.Ile689=)	rs61266641	0.00789
NM_001171.6(ABCC6):c.4254G>A (p.Arg1418=)	rs58668703	0.00784
NM_001171.6(ABCC6):c.2707G>C (p.Glu903Gln)	rs60712230	0.00774
NM_001171.6(ABCC6):c.3980G>A (p.Gly1327Glu)	rs57695665	0.00432
NM_001171.6(ABCC6):c.1248C>T (p.Asp416=)	rs143487365	0.00247
NM_001171.6(ABCC6):c.1284C>T (p.Asn428=)	rs57499497	0.00245
NM_001171.6(ABCC6):c.1263C>T (p.Thr421=)	rs114179357	0.00180
NM_001171.6(ABCC6):c.2781C>T (p.Tyr927=)	rs61731973	0.00153
NM_001171.6(ABCC6):c.2904G>A (p.Leu968=)	rs72664287	0.00087
NM_001171.6(ABCC6):c.179G>A (p.Arg60Gln)	rs183648123	0.00003
NM_001171.6(ABCC6):c.1338+20C>G	rs12929920

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.