List of variants reported as pathogenic for Andersen Tawil syndrome by OMIM

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.161G>T (p.Cys54Phe)	rs199473650
NM_000891.3(KCNJ2):c.199C>T (p.Arg67Trp)	rs104894580
NM_000891.3(KCNJ2):c.212A>T (p.Asp71Val)	rs104894575
NM_000891.3(KCNJ2):c.224C>G (p.Thr75Arg)	rs104894585
NM_000891.3(KCNJ2):c.285_296del (p.Trp96_Phe99del)	rs2144376746
NM_000891.3(KCNJ2):c.557C>T (p.Pro186Leu)	rs104894581
NM_000891.3(KCNJ2):c.646A>C (p.Asn216His)	rs104894583
NM_000891.3(KCNJ2):c.652C>T (p.Arg218Trp)	rs104894578
NM_000891.3(KCNJ2):c.899G>T (p.Gly300Val)	rs104894579
NM_000891.3(KCNJ2):c.904G>A (p.Val302Met)	rs104894582
NM_000891.3(KCNJ2):c.913A>C (p.Thr305Pro)	rs199473387
NM_000891.3(KCNJ2):c.939_944del (p.Ser314_Tyr315del)	rs2074390325

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