ClinVar Miner

List of variants reported as likely benign for alopecia, isolated

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_005144.5(HR):c.1859G>A (p.Arg620Gln) rs117197822 0.02084
NM_005144.5(HR):c.*82G>T rs112057122 0.01214
NM_005144.5(HR):c.*75G>A rs114993748 0.00298
NM_005144.5(HR):c.2862T>A (p.Ala954=) rs148407688 0.00225
NM_005144.5(HR):c.1557-13G>A rs113141789 0.00205
NM_005144.5(HR):c.1517A>G (p.Glu506Gly) rs112016555 0.00203
NM_005144.5(HR):c.3250G>A (p.Ala1084Thr) rs201956860 0.00177
NM_005144.5(HR):c.3507+12G>A rs79262499 0.00140
NM_005144.5(HR):c.333C>T (p.Cys111=) rs143223831 0.00034
NM_005144.5(HR):c.3470C>G (p.Pro1157Arg) rs201030061 0.00014
NM_005144.5(HR):c.*894G>A rs564636595 0.00009
NM_005144.5(HR):c.301G>A (p.Glu101Lys) rs28585381 0.00003
NM_005144.5(HR):c.2507G>T (p.Arg836Leu) rs201739936
NM_005144.5(HR):c.3249C>A (p.Gly1083=) rs552153164
NM_005144.5(HR):c.37A>G (p.Thr13Ala) rs143316642

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