ClinVar Miner

List of variants reported as benign for Marie Unna hereditary hypotrichosis

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 44
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HGVS dbSNP
NM_005144.4(HR):c.*1251dup rs11446222
NM_005144.4(HR):c.*218T>C rs74869265
NM_005144.4(HR):c.*240C>A rs6994872
NM_005144.4(HR):c.*81C>T rs114329519
NM_005144.4(HR):c.*820G>C rs142767236
NM_005144.4(HR):c.*931T>C rs76436208
NM_005144.4(HR):c.-333T>C rs147674174
NM_005144.4(HR):c.-615T>G rs6557841
NM_005144.4(HR):c.1010G>A (p.Gly337Asp) rs12675375
NM_005144.4(HR):c.1055C>T (p.Ala352Val) rs115396678
NM_005144.4(HR):c.1190G>A (p.Cys397Tyr) rs73549523
NM_005144.4(HR):c.1305T>C (p.Phe435=) rs12675745
NM_005144.4(HR):c.1461C>T (p.Cys487=) rs78703240
NM_005144.4(HR):c.1507G>A (p.Ala503Thr) rs115643651
NM_005144.4(HR):c.1572G>A (p.Gly524=) rs149811800
NM_005144.4(HR):c.1577T>C (p.Leu526Pro) rs56140348
NM_005144.4(HR):c.1583A>G (p.Gln528Arg) rs74596676
NM_005144.4(HR):c.1858C>G (p.Arg620Gly) rs200843097
NM_005144.4(HR):c.188C>G (p.Pro63Arg) rs73549525
NM_005144.4(HR):c.1907A>G (p.Glu636Gly) rs75362423
NM_005144.4(HR):c.205C>T (p.Pro69Ser)
NM_005144.4(HR):c.2104G>T (p.Gly702Trp) rs138941448
NM_005144.4(HR):c.2211C>T (p.Pro737=) rs77689228
NM_005144.4(HR):c.2367T>C (p.Ser789=) rs58080661
NM_005144.4(HR):c.2370T>C (p.Asp790=) rs57903149
NM_005144.4(HR):c.2467G>A (p.Gly823Ser) rs76547188
NM_005144.4(HR):c.2526A>C (p.Pro842=) rs371431900
NM_005144.4(HR):c.2570G>A (p.Arg857His) rs114871775
NM_005144.4(HR):c.2617T>C (p.Leu873=) rs116376389
NM_005144.4(HR):c.2733C>A (p.Ser911Arg) rs11990451
NM_005144.4(HR):c.27G>A (p.Lys9=) rs77620102
NM_005144.4(HR):c.3064A>G (p.Thr1022Ala) rs7014851
NM_005144.4(HR):c.3192C>T (p.Arg1064=) rs114507110
NM_005144.4(HR):c.3213+10C>T rs116703265
NM_005144.4(HR):c.3339C>A (p.Pro1113=) rs112173147
NM_005144.4(HR):c.956C>T (p.Pro319Leu) rs77758962
NM_005144.5(HR):c.*599T>G
NM_005144.5(HR):c.*756G>T
NM_005144.5(HR):c.1359G>A (p.Ser453=)
NM_005144.5(HR):c.1380C>T (p.Asp460=)
NM_005144.5(HR):c.1727C>T (p.Ala576Val)
NM_005144.5(HR):c.1956C>T (p.Ala652=)
NM_005144.5(HR):c.3216G>A (p.Val1072=)
NM_005144.5(HR):c.3253C>G (p.Pro1085Ala)

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