ClinVar Miner

List of variants in gene SLC12A2 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001046.3(SLC12A2):c.2006-90C>T rs2617618 0.99886
NM_001046.3(SLC12A2):c.1048+208T>A rs3816006 0.35592
NM_001046.3(SLC12A2):c.1191A>G (p.Glu397=) rs2228112 0.35370
NM_001046.3(SLC12A2):c.756+298T>C rs1864922 0.35339
NM_001046.3(SLC12A2):c.1622-104T>C rs3805607 0.32053
NM_001046.3(SLC12A2):c.1881+176A>G rs73337363 0.32024
NM_001046.3(SLC12A2):c.2977+29A>C rs1559263 0.30499
NM_001046.3(SLC12A2):c.3213-242C>T rs10463838 0.29734
NM_001046.3(SLC12A2):c.2723+222C>T rs59484271 0.26175
NM_001046.3(SLC12A2):c.3100+55A>T rs17764954 0.22590
NM_001046.3(SLC12A2):c.2364-66A>G rs17164310 0.20976
NM_001046.3(SLC12A2):c.*220C>T rs10089 0.20916
NM_001046.3(SLC12A2):c.2723+220T>C rs7720888 0.05129
NM_001046.3(SLC12A2):c.2364-51G>A rs73784521 0.05091
NM_001046.3(SLC12A2):c.3212+14A>C rs10519975 0.04237
NM_001046.3(SLC12A2):c.1189-136A>G rs79273460 0.02996
NM_001046.3(SLC12A2):c.1299+135G>A rs41298324 0.02304
NM_001046.3(SLC12A2):c.1300-238G>A rs6875842 0.01996
NM_001046.3(SLC12A2):c.524G>C (p.Gly175Ala) rs149585221 0.00499
NM_001046.3(SLC12A2):c.2322A>C (p.Ser774=) rs115357531 0.00153
NM_001046.3(SLC12A2):c.2380A>G (p.Met794Val) rs116191759 0.00103
NM_001046.3(SLC12A2):c.3468A>G (p.Leu1156=) rs115092488 0.00098
NM_001046.3(SLC12A2):c.876+17_876+18del rs556046317 0.00094
NM_001046.3(SLC12A2):c.2748A>T (p.Gly916=) rs141683516 0.00080
NM_001046.3(SLC12A2):c.2005+9T>C rs10463502 0.00071
NM_001046.3(SLC12A2):c.3100+13A>T rs199929591 0.00066
NM_001046.3(SLC12A2):c.495C>T (p.Asp165=) rs138234695 0.00051
NM_001046.3(SLC12A2):c.953-7C>T rs201608609 0.00044
NM_001046.3(SLC12A2):c.957A>G (p.Leu319=) rs115395895 0.00006
NM_001046.3(SLC12A2):c.1188+214A>T rs891886
NM_001046.3(SLC12A2):c.1566A>G (p.Thr522=)
NM_001046.3(SLC12A2):c.1881+181_1881+184dup rs111466483
NM_001046.3(SLC12A2):c.2107+11A>G rs189093520
NM_001046.3(SLC12A2):c.2217T>C (p.Tyr739=)
NM_001046.3(SLC12A2):c.2263+172del rs11331893
NM_001046.3(SLC12A2):c.2263+17G>A
NM_001046.3(SLC12A2):c.2723+221AC[6] rs72198423
NM_001046.3(SLC12A2):c.2804-115_2804-113del rs150215270
NM_001046.3(SLC12A2):c.2897A>T (p.Lys966Ile)
NM_001046.3(SLC12A2):c.2984A>G (p.Lys995Arg)
NM_001046.3(SLC12A2):c.3390A>G (p.Glu1130=)
NM_001046.3(SLC12A2):c.3504-23dup rs11382084
NM_001046.3(SLC12A2):c.534G>C (p.Val178=)
NM_001046.3(SLC12A2):c.681C>T (p.Tyr227=)

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.