ClinVar Miner

List of variants in gene SLC9A6 reported as benign for Christianson syndrome

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1306+8G>A rs6654310 0.05510
NM_001379110.1(SLC9A6):c.1689C>T (p.Ser563=) rs2307131 0.02758
NM_001379110.1(SLC9A6):c.744-6C>T rs17001258 0.01856
NM_001379110.1(SLC9A6):c.1662-4G>A rs188072063 0.00703
NM_001379110.1(SLC9A6):c.474T>C (p.Ser158=) rs144316388 0.00662
NM_001379110.1(SLC9A6):c.1029A>C (p.Ala343=) rs142049079 0.00390
NM_001379110.1(SLC9A6):c.1460+4A>G rs180727016 0.00239
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln) rs146263125 0.00166
NM_001379110.1(SLC9A6):c.*8A>T rs200171451 0.00157
NM_001379110.1(SLC9A6):c.1460+6T>C rs781963949 0.00047
NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=) rs151178361 0.00022
NM_001379110.1(SLC9A6):c.1460+10A>G rs185533973 0.00013
NM_001379110.1(SLC9A6):c.1581+11G>A rs375145994 0.00012
NM_001379110.1(SLC9A6):c.2022G>A (p.Thr674=) rs781885129 0.00010
NM_001379110.1(SLC9A6):c.170-16T>A rs548206389 0.00006
NM_001379110.1(SLC9A6):c.1005A>G (p.Val335=) rs782706500 0.00004
NM_001379110.1(SLC9A6):c.1307-12G>C rs372153079 0.00003
NM_001379110.1(SLC9A6):c.1887A>G (p.Arg629=) rs782350079 0.00003
NM_001379110.1(SLC9A6):c.1922G>A (p.Arg641Gln) rs781912974 0.00003
NM_001379110.1(SLC9A6):c.486C>T (p.Tyr162=) rs782176162 0.00003
NM_001379110.1(SLC9A6):c.564G>A (p.Thr188=) rs782216766 0.00003
NM_001379110.1(SLC9A6):c.-56-35C>G rs1282592417 0.00002
NM_001379110.1(SLC9A6):c.1080+10A>G rs191388209 0.00002
NM_001379110.1(SLC9A6):c.220G>A (p.Val74Ile) rs781798443 0.00002
NM_001379110.1(SLC9A6):c.-4A>G rs782090744 0.00001
NM_001379110.1(SLC9A6):c.2001G>A (p.Pro667=) rs782708610 0.00001
NM_001379110.1(SLC9A6):c.57C>T (p.Ser19=) rs781963863 0.00001
NM_001379110.1(SLC9A6):c.1059G>A (p.Glu353=)
NM_001379110.1(SLC9A6):c.1080+80dup rs35492327
NM_001379110.1(SLC9A6):c.1307-13T>C
NM_001379110.1(SLC9A6):c.1581+16del
NM_001379110.1(SLC9A6):c.1582-3C>T rs563279759
NM_001379110.1(SLC9A6):c.1661+28del rs376371956
NM_001379110.1(SLC9A6):c.1661+28dup rs376371956
NM_001379110.1(SLC9A6):c.448-6del rs375038684
NM_001379110.1(SLC9A6):c.448-6dup rs375038684
NM_001379110.1(SLC9A6):c.448-7_448-6dup rs375038684
NM_001379110.1(SLC9A6):c.638-10dup rs2089592364

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