List of variants reported as uncertain significance for Dent disease type 1 by Illumina Clinical Services Laboratory,Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 61

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HGVS	dbSNP
NM_001127898.4(CLCN5):c.*1292C>T	rs781855238
NM_001127898.4(CLCN5):c.*1339A>G
NM_001127898.4(CLCN5):c.*1625C>T
NM_001127898.4(CLCN5):c.*1868T>C
NM_001127898.4(CLCN5):c.*1874G>A	rs1053041096
NM_001127898.4(CLCN5):c.*1887G>C
NM_001127898.4(CLCN5):c.*1938G>A
NM_001127898.4(CLCN5):c.*2270A>G	rs1057515936
NM_001127898.4(CLCN5):c.*2317G>A	rs969354356
NM_001127898.4(CLCN5):c.*2324G>A	rs782677531
NM_001127898.4(CLCN5):c.*2384A>C
NM_001127898.4(CLCN5):c.*2460G>A	rs111452206
NM_001127898.4(CLCN5):c.*2479G>A	rs782387568
NM_001127898.4(CLCN5):c.*2557A>G	rs1057515938
NM_001127898.4(CLCN5):c.*2849C>T
NM_001127898.4(CLCN5):c.*2980A>G	rs56147923
NM_001127898.4(CLCN5):c.*3071A>G	rs1057515939
NM_001127898.4(CLCN5):c.*3090C>T	rs1057515940
NM_001127898.4(CLCN5):c.*3091G>A
NM_001127898.4(CLCN5):c.*3388T>G
NM_001127898.4(CLCN5):c.*3495A>G	rs183523710
NM_001127898.4(CLCN5):c.*3627C>T	rs1057515941
NM_001127898.4(CLCN5):c.*379G>C
NM_001127898.4(CLCN5):c.*3912C>T
NM_001127898.4(CLCN5):c.*3937C>A	rs1057515942
NM_001127898.4(CLCN5):c.*3957C>G
NM_001127898.4(CLCN5):c.*39C>T
NM_001127898.4(CLCN5):c.*4034A>T	rs782274908
NM_001127898.4(CLCN5):c.*4297A>C	rs868964422
NM_001127898.4(CLCN5):c.*4606A>C
NM_001127898.4(CLCN5):c.*4740C>G
NM_001127898.4(CLCN5):c.*477G>A	rs1035298488
NM_001127898.4(CLCN5):c.*4911G>A
NM_001127898.4(CLCN5):c.*504G>C	rs1057515931
NM_001127898.4(CLCN5):c.*5088G>T
NM_001127898.4(CLCN5):c.*5240T>C
NM_001127898.4(CLCN5):c.*5340A>C
NM_001127898.4(CLCN5):c.*5377G>A
NM_001127898.4(CLCN5):c.*5815T>C	rs1057515945
NM_001127898.4(CLCN5):c.*5844C>T
NM_001127898.4(CLCN5):c.*5895T>A	rs1057515947
NM_001127898.4(CLCN5):c.*5970C>T
NM_001127898.4(CLCN5):c.*6163T>C
NM_001127898.4(CLCN5):c.*6217G>A	rs781967731
NM_001127898.4(CLCN5):c.*6240G>C	rs782177733
NM_001127898.4(CLCN5):c.*6482C>T
NM_001127898.4(CLCN5):c.*6608C>T	rs1016988265
NM_001127898.4(CLCN5):c.*6638G>A	rs963123113
NM_001127898.4(CLCN5):c.*6694C>T
NM_001127898.4(CLCN5):c.*6841T>C
NM_001127898.4(CLCN5):c.*866A>G
NM_001127898.4(CLCN5):c.*969A>G
NM_001127898.4(CLCN5):c.164-2118G>T	rs957427726
NM_001127898.4(CLCN5):c.164-2130C>T
NM_001127898.4(CLCN5):c.164-2249C>T	rs781792158
NM_001127898.4(CLCN5):c.164-2276G>A	rs905143179
NM_001127898.4(CLCN5):c.1872G>A (p.Arg624=)
NM_001127898.4(CLCN5):c.2293C>T (p.Pro765Ser)
NM_001127898.4(CLCN5):c.2305G>A (p.Val769Ile)	rs201962580
NM_001127898.4(CLCN5):c.448C>A (p.His150Asn)
NM_001127898.4(CLCN5):c.696G>A (p.Ala232=)	rs140312372

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