ClinVar Miner

List of variants in gene FOXRED1 reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (168):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_017547.3(FOXRED1):c.-163G>C rs552937899
NM_017547.4(FOXRED1):c.*159C>T rs570233921
NM_017547.4(FOXRED1):c.*190T>C rs77902129
NM_017547.4(FOXRED1):c.*392G>A rs886047983
NM_017547.4(FOXRED1):c.*432T>G rs185024577
NM_017547.4(FOXRED1):c.*85T>C rs372575072
NM_017547.4(FOXRED1):c.-31A>G rs368307265
NM_017547.4(FOXRED1):c.1020G>C (p.Pro340=) rs143739550
NM_017547.4(FOXRED1):c.10A>G (p.Arg4Gly) rs149883459
NM_017547.4(FOXRED1):c.1138C>G (p.His380Asp) rs751634994
NM_017547.4(FOXRED1):c.1139A>G (p.His380Arg) rs7116126
NM_017547.4(FOXRED1):c.1171T>G (p.Leu391Val) rs138061928
NM_017547.4(FOXRED1):c.1183G>T (p.Val395Phe) rs767749700
NM_017547.4(FOXRED1):c.124A>C (p.Lys42Gln) rs148346044
NM_017547.4(FOXRED1):c.192G>A (p.Ser64=) rs749675822
NM_017547.4(FOXRED1):c.296G>A (p.Arg99Gln) rs768102112
NM_017547.4(FOXRED1):c.305C>T (p.Thr102Met) rs77785510
NM_017547.4(FOXRED1):c.35G>C (p.Arg12Pro) rs375454069
NM_017547.4(FOXRED1):c.418-1G>T rs771941278
NM_017547.4(FOXRED1):c.433G>A (p.Val145Ile) rs34542988
NM_017547.4(FOXRED1):c.435C>T (p.Val145=) rs147235743
NM_017547.4(FOXRED1):c.568C>T (p.Pro190Ser) rs1555065162
NM_017547.4(FOXRED1):c.580C>T (p.Arg194Trp) rs191604046
NM_017547.4(FOXRED1):c.612_615dup (p.Ala206fs) rs398124308
NM_017547.4(FOXRED1):c.658C>T (p.Pro220Ser) rs753106152
NM_017547.4(FOXRED1):c.662G>T (p.Trp221Leu) rs755831680
NM_017547.4(FOXRED1):c.754C>T (p.Arg252Cys) rs146661281
NM_017547.4(FOXRED1):c.833A>G (p.Glu278Gly) rs886047981
NM_017547.4(FOXRED1):c.857T>C (p.Ile286Thr) rs148955548
NM_017547.4(FOXRED1):c.887C>T (p.Ala296Val) rs886047982
NM_017547.4(FOXRED1):c.921G>A (p.Gly307=) rs777315728
NM_017547.4(FOXRED1):c.952C>T (p.Pro318Ser) rs748195712
NM_017547.4(FOXRED1):c.9G>A (p.Arg3=) rs28372779

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