ClinVar Miner

List of variants reported as benign for specific language disorder by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_014491.4(FOXP2):c.*2265G>T rs12705977 0.33362
NM_014491.4(FOXP2):c.*3683C>T rs1058335 0.16716
NM_014491.4(FOXP2):c.*3822C>T rs10244649 0.12102
NM_014491.4(FOXP2):c.*205_*206insC rs766446822 0.02729
NM_014491.4(FOXP2):c.741C>T (p.Gly247=) rs61732741 0.01128
NM_014491.4(FOXP2):c.531A>G (p.Gln177=) rs111801240 0.01115
NM_014491.4(FOXP2):c.570A>G (p.Gln190=) rs61758964 0.01012
NM_014491.4(FOXP2):c.*2253A>T rs73210755 0.00936
NM_014491.4(FOXP2):c.-99G>A rs116320717 0.00774
NM_014491.4(FOXP2):c.*2017G>A rs75054333 0.00583
NM_014491.4(FOXP2):c.*3199G>A rs149254099 0.00537
NM_014491.4(FOXP2):c.*3624T>G rs540406830 0.00376
NM_014491.4(FOXP2):c.*3563C>T rs148596176 0.00342
NM_014491.4(FOXP2):c.1468+9T>C rs75753538 0.00294
NM_014491.4(FOXP2):c.*80A>G rs550961565 0.00239
NM_014491.4(FOXP2):c.552A>G (p.Gln184=) rs146945410 0.00209
NM_014491.4(FOXP2):c.*2082A>G rs145961115 0.00203
NM_014491.4(FOXP2):c.*998A>G rs181206486 0.00136
NM_014491.4(FOXP2):c.*3517T>C rs79694890 0.00123
NM_014491.4(FOXP2):c.*207T>C rs776533754 0.00109
NM_014491.4(FOXP2):c.*3466G>A rs544350916 0.00108
NM_014491.4(FOXP2):c.*2571C>T rs575232403 0.00094
NM_014491.4(FOXP2):c.*276A>G rs531205756 0.00092
NM_014491.4(FOXP2):c.*2018A>G rs768026922 0.00056
NM_014491.4(FOXP2):c.1371T>C (p.Ile457=) rs61753357 0.00046
NM_014491.4(FOXP2):c.1770-14A>T rs554154151 0.00043
NM_014491.4(FOXP2):c.*236A>G rs775524542 0.00038
NM_014491.4(FOXP2):c.*3457G>A rs190599917 0.00036
NM_014491.4(FOXP2):c.*206T>C rs563988777 0.00033
NM_014491.4(FOXP2):c.*515A>T rs150361315 0.00032
NM_014491.4(FOXP2):c.*1944C>T rs142461550 0.00030
NM_014491.4(FOXP2):c.1266+8C>T rs139649711 0.00030
NM_014491.4(FOXP2):c.1431G>A (p.Arg477=) rs148518030 0.00024
NM_014491.4(FOXP2):c.*2818G>C rs532545326 0.00020
NM_014491.4(FOXP2):c.1770-12T>A rs771960652 0.00014
NM_014491.4(FOXP2):c.*1969T>A rs771063685 0.00011
NM_014491.4(FOXP2):c.598-10C>T rs369461083 0.00009
NM_014491.4(FOXP2):c.*1945G>A rs185964187 0.00007
NM_014491.4(FOXP2):c.1494T>C (p.Tyr498=) rs191237950 0.00007
NM_014491.4(FOXP2):c.1686T>C (p.Phe562=) rs372567072 0.00004
NM_014491.4(FOXP2):c.*3423C>T rs117309491 0.00003
NM_014491.4(FOXP2):c.-14G>T rs759420480 0.00003
NM_014491.4(FOXP2):c.*250A>G rs368786145 0.00002
NM_014491.4(FOXP2):c.1441G>A (p.Asp481Asn) rs755825043 0.00001
NM_014491.4(FOXP2):c.522A>G (p.Gln174=) rs368614280 0.00001
NM_014491.3(FOXP2):c.618_620dupGCA
NM_014491.4(FOXP2):c.*2030del rs750710459
NM_014491.4(FOXP2):c.*2191C>T rs114784365
NM_014491.4(FOXP2):c.*229dup rs543811999
NM_014491.4(FOXP2):c.*260del rs752684219
NM_014491.4(FOXP2):c.*2965T>C rs530179782
NM_014491.4(FOXP2):c.1982G>A (p.Gly661Asp) rs529427719

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