ClinVar Miner

List of variants reported as benign for alopecia, isolated

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001394132.1(HRURF):c.-294T>G rs6557841 0.65210
NM_005144.5(HR):c.1305T>C (p.Phe435=) rs12675745 0.63572
NM_005144.5(HR):c.*240C>A rs6994872 0.37740
NM_005144.5(HR):c.3379-29G>T rs6557829 0.35485
NM_005144.5(HR):c.1010G>A (p.Gly337Asp) rs12675375 0.28084
NM_005144.5(HR):c.1577T>C (p.Leu526Pro) rs56140348 0.19328
NM_005144.5(HR):c.2370T>C (p.Asp790=) rs57903149 0.11618
NM_005144.5(HR):c.2367T>C (p.Ser789=) rs58080661 0.11568
NM_005144.5(HR):c.3064A>G (p.Thr1022Ala) rs7014851 0.08773
NM_005144.5(HR):c.1583A>G (p.Gln528Arg) rs74596676 0.07210
NM_005144.5(HR):c.1190G>A (p.Cys397Tyr) rs73549523 0.06592
NM_005144.5(HR):c.2733C>A (p.Ser911Arg) rs11990451 0.05556
NM_005144.5(HR):c.956C>T (p.Pro319Leu) rs77758962 0.05449
NM_005144.5(HR):c.188C>G (p.Pro63Arg) rs73549525 0.03073
NM_005144.5(HR):c.27G>A (p.Lys9=) rs77620102 0.03021
NM_005144.5(HR):c.*820G>C rs142767236 0.01950
NM_005144.5(HR):c.2467G>A (p.Gly823Ser) rs76547188 0.01641
NM_001394132.1(HRURF):c.-12T>C rs147674174 0.01614
NM_005144.5(HR):c.1507G>A (p.Ala503Thr) rs115643651 0.01594
NM_005144.5(HR):c.2570G>A (p.Arg857His) rs114871775 0.01509
NM_005144.5(HR):c.1055C>T (p.Ala352Val) rs115396678 0.01418
NM_005144.5(HR):c.*81C>T rs114329519 0.01316
NM_005144.5(HR):c.2211C>T (p.Pro737=) rs77689228 0.01241
NM_005144.5(HR):c.*218T>C rs74869265 0.01220
NM_005144.5(HR):c.1907A>G (p.Glu636Gly) rs75362423 0.01168
NM_005144.5(HR):c.1461C>T (p.Cys487=) rs78703240 0.01153
NM_005144.5(HR):c.*599T>G rs76109349 0.01096
NM_005144.5(HR):c.1359G>A (p.Ser453=) rs78489044 0.00909
NM_005144.5(HR):c.3216G>A (p.Val1072=) rs146855847 0.00634
NM_005144.5(HR):c.3253C>G (p.Pro1085Ala) rs143782421 0.00633
NM_005144.5(HR):c.*756G>T rs116456103 0.00573
NM_005144.5(HR):c.2617T>C (p.Leu873=) rs116376389 0.00542
NM_005144.5(HR):c.3192C>T (p.Arg1064=) rs114507110 0.00527
NM_005144.5(HR):c.3213+10C>T rs116703265 0.00522
NM_005144.5(HR):c.1727C>T (p.Ala576Val) rs76294724 0.00512
NM_005144.5(HR):c.205C>T (p.Pro69Ser) rs78621054 0.00328
NM_005144.5(HR):c.*931T>C rs76436208 0.00289
NM_005144.5(HR):c.1956C>T (p.Ala652=) rs78939934 0.00264
NM_005144.5(HR):c.2526A>C (p.Pro842=) rs371431900 0.00199
NM_005144.5(HR):c.1380C>T (p.Asp460=) rs147308644 0.00196
NM_005144.5(HR):c.2104G>T (p.Gly702Trp) rs138941448 0.00134
NM_005144.5(HR):c.1572G>A (p.Gly524=) rs149811800 0.00050
NM_005144.5(HR):c.*1251dup rs11446222
NM_005144.5(HR):c.1858C>G (p.Arg620Gly) rs200843097
NM_005144.5(HR):c.3339C>A (p.Pro1113=) rs112173147

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