ClinVar Miner

List of variants in gene FIG4 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
GRCh37/hg19 6q21(chr6:110050042-110117170)x3
NM_014845.5(FIG4):c.1138-175G>T rs80101079
NM_014845.5(FIG4):c.122T>C (p.Ile41Thr) rs121908287
NM_014845.5(FIG4):c.1272-238C>T rs7756284
NM_014845.5(FIG4):c.1434+181G>T rs13196280
NM_014845.5(FIG4):c.1434+238T>C rs6912209
NM_014845.5(FIG4):c.1584-317T>C rs17612996
NM_014845.5(FIG4):c.1584-8T>A rs199522051
NM_014845.5(FIG4):c.165+100A>T rs6924436
NM_014845.5(FIG4):c.173A>G (p.Tyr58Cys) rs145337669
NM_014845.5(FIG4):c.1948+46C>A rs9320315
NM_014845.5(FIG4):c.1949-308G>A rs9386844
NM_014845.5(FIG4):c.1961T>C (p.Val654Ala) rs9885672
NM_014845.5(FIG4):c.2097-243A>C rs9386845
NM_014845.5(FIG4):c.2180+63G>T rs9384723
NM_014845.5(FIG4):c.2460-252A>G rs72944977
NM_014845.5(FIG4):c.27C>T (p.Ile9=) rs141040807
NM_014845.5(FIG4):c.289+331G>A rs7771150
NM_014845.5(FIG4):c.290-147C>T rs6921615
NM_014845.5(FIG4):c.447-119T>G rs11153215
NM_014845.5(FIG4):c.66+10C>T rs200063827
NM_014845.5(FIG4):c.775+298G>A rs12201444
NM_014845.5(FIG4):c.876+126T>G rs1322124

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