ClinVar Miner

List of variants in gene KCNQ3 reported as benign for not provided

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Gene type:
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Total variants: 33
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HGVS dbSNP
GRCh37/hg19 8q24.22(chr8:133226397-133306801)x1
NM_004519.4(KCNQ3):c.-142G>T rs28606540
NM_004519.4(KCNQ3):c.-318G>A rs577534558
NM_004519.4(KCNQ3):c.-504A>G rs71512326
NM_004519.4(KCNQ3):c.-519C>G rs71512327
NM_004519.4(KCNQ3):c.-556T>G rs2597367
NM_004519.4(KCNQ3):c.1044+156A>G rs62519574
NM_004519.4(KCNQ3):c.1235+38A>G rs4736555
NM_004519.4(KCNQ3):c.1236-134C>T rs73355088
NM_004519.4(KCNQ3):c.1236-64C>T rs17653354
NM_004519.4(KCNQ3):c.1262+269T>C rs1432030
NM_004519.4(KCNQ3):c.1465+256A>G rs1864769
NM_004519.4(KCNQ3):c.1568+12A>G rs181790623
NM_004519.4(KCNQ3):c.1700+29G>A rs2469515
NM_004519.4(KCNQ3):c.1700+3G>A rs115092422
NM_004519.4(KCNQ3):c.1885-110C>T rs2436132
NM_004519.4(KCNQ3):c.1885-67C>G rs2469625
NM_004519.4(KCNQ3):c.2306C>A (p.Pro769His) rs114095081
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831
NM_004519.4(KCNQ3):c.386+32845T>C rs72721077
NM_004519.4(KCNQ3):c.605-302C>T rs76474027
NM_004519.4(KCNQ3):c.777+121C>T rs41272385
NM_004519.4(KCNQ3):c.777+135A>G rs41272383
NM_004519.4(KCNQ3):c.777+220G>C rs41272381
NM_004519.4(KCNQ3):c.777+225G>C rs41272379
NM_004519.4(KCNQ3):c.777+306G>C rs76215494
NM_004519.4(KCNQ3):c.778-203T>G rs10505591
NM_004519.4(KCNQ3):c.933+114G>A rs16904620
NM_004519.4(KCNQ3):c.933+128A>T rs75870584
NM_004519.4(KCNQ3):c.933+129A>C rs77494140
NM_004519.4(KCNQ3):c.933+25T>C rs17575971
NM_004519.4(KCNQ3):c.934-108G>A rs17653902
NM_004519.4(KCNQ3):c.934-228C>T rs10505590

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