ClinVar Miner

List of variants reported as uncertain significance for Focal segmental glomerulosclerosis 8

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_018685.5(ANLN):c.31C>T (p.Arg11Ter) rs200989750 0.00025
NM_018685.5(ANLN):c.524C>T (p.Pro175Leu) rs148482760 0.00022
NM_018685.5(ANLN):c.752G>A (p.Ser251Asn) rs372980930 0.00019
NM_018685.5(ANLN):c.1127G>A (p.Arg376His) rs368703385 0.00004
NM_018685.5(ANLN):c.1171C>T (p.Arg391Cys) rs562511350 0.00004
NM_018685.5(ANLN):c.191C>G (p.Pro64Arg) rs200238245 0.00003
NM_018685.5(ANLN):c.1138C>T (p.Arg380Cys) rs201613256 0.00002
NM_018685.5(ANLN):c.2440A>G (p.Lys814Glu) rs778238903 0.00001
NM_007286.6(SYNPO):c.1808C>T (p.Pro603Leu) rs1464796596
NM_018685.5(ANLN):c.1547A>T (p.Lys516Ile)
NM_018685.5(ANLN):c.1588A>C (p.Lys530Gln) rs2116638569
NM_018685.5(ANLN):c.1979A>G (p.Asp660Gly) rs1787820175
NM_018685.5(ANLN):c.2405del (p.Gly802fs) rs1787929800
NM_018685.5(ANLN):c.28G>A (p.Glu10Lys)
NM_018685.5(ANLN):c.3035A>T (p.Asn1012Ile)
NM_018685.5(ANLN):c.3158G>A (p.Arg1053His)
NM_018685.5(ANLN):c.65A>G (p.Lys22Arg) rs2116507412
NM_018685.5(ANLN):c.896C>A (p.Ser299Tyr)

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