ClinVar Miner

List of variants reported as not provided for Hypotension

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Total variants: 28
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HGVS dbSNP
NM_001300.6(KLF6):c.*46A>T rs483352821
NM_001300.6(KLF6):c.*62G>A rs112418040
NM_001300.6(KLF6):c.496C>T (p.Pro166Ser) rs142749289
NM_001300.6(KLF6):c.603G>A (p.Arg201=) rs112847236
NM_001300.6(KLF6):c.800+21C>T rs111743412
NM_001300.6(KLF6):c.800+34G>A rs367807577
NM_001818.4(AKR1C4):c.447+9T>G rs201441444
NM_003739.6(AKR1C3):c.643G>A (p.Ala215Thr) rs483352820
NM_017637.6(BNC2):c.1002A>G (p.Pro334=) rs483353010
NM_017637.6(BNC2):c.1239T>C (p.Asp413=) rs483353011
NM_017637.6(BNC2):c.1240C>G (p.Leu414Val) rs148873573
NM_017637.6(BNC2):c.1545A>G (p.Ser515=) rs117470554
NM_017637.6(BNC2):c.171G>T (p.Gln57His) rs145011045
NM_017637.6(BNC2):c.1738G>A (p.Gly580Arg) rs483353012
NM_017637.6(BNC2):c.1868C>A (p.Pro623His) rs114596065
NM_017637.6(BNC2):c.1947C>T (p.Thr649=) rs62540608
NM_017637.6(BNC2):c.2051C>T (p.Pro684Leu) rs138187836
NM_017637.6(BNC2):c.2202C>T (p.Gly734=) rs376030025
NM_017637.6(BNC2):c.2478A>G (p.Leu826=) rs3739715
NM_017637.6(BNC2):c.2739C>T (p.Arg913=) rs189895388
NM_017637.6(BNC2):c.2768C>T (p.Ala923Val) rs117452684
NM_017637.6(BNC2):c.2789A>G (p.Asp930Gly) rs41268965
NM_017637.6(BNC2):c.2920A>G (p.Ile974Val) rs35005898
NM_017637.6(BNC2):c.501C>T (p.Val167=) rs143821778
NM_017637.6(BNC2):c.519C>T (p.Ser173=) rs149019822
NM_017637.6(BNC2):c.84A>T (p.Ala28=) rs76485966
NM_017637.6(BNC2):c.916C>G (p.Pro306Ala) rs114964332
NM_017637.6(BNC2):c.936C>T (p.Phe312=) rs77464990

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