ClinVar Miner

List of variants reported as benign for autosomal recessive nonsyndromic hearing loss 2 by Genome-Nilou Lab

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_000260.4(MYO7A):c.6558+51G>T rs948959 0.92365
NM_000260.4(MYO7A):c.6438+50A>T rs2276289 0.86951
NM_000260.4(MYO7A):c.5743-12T>C rs2276291 0.63742
NM_000260.4(MYO7A):c.5944+57G>A rs948961 0.63248
NM_000260.4(MYO7A):c.3750+89C>T rs2276286 0.63230
NM_000260.4(MYO7A):c.2905-54A>G rs7117606 0.62793
NM_000260.4(MYO7A):c.3751-94C>G rs7947922 0.62425
NM_000260.4(MYO7A):c.2367+67T>C rs10793239 0.60184
NM_000260.4(MYO7A):c.4996A>T (p.Ser1666Cys) rs2276288 0.59864
NM_000260.4(MYO7A):c.4324-207C>G rs12802853 0.59234
NM_000260.4(MYO7A):c.4324-202A>G rs12421897 0.59230
NM_000260.4(MYO7A):c.4323+35G>T rs1109977 0.59156
NM_000260.4(MYO7A):c.5637-175A>G rs4945160 0.59068
NM_000260.4(MYO7A):c.5480+162C>G rs11237120 0.59043
NM_000260.4(MYO7A):c.5481-83A>G rs11237121 0.58275
NM_000260.4(MYO7A):c.5856+50G>A rs2276290 0.56770
NM_000260.4(MYO7A):c.5715A>G (p.Lys1905=) rs2276293 0.56709
NM_000260.4(MYO7A):c.6051+17T>A rs1320702 0.56699
NM_000260.4(MYO7A):c.5857-7A>T rs1320703 0.56654
NM_000260.4(MYO7A):c.5944+67C>T rs948960 0.56521
NM_000260.4(MYO7A):c.1936-23G>A rs2276283 0.52888
NM_000260.4(MYO7A):c.3924+12C>T rs2276285 0.51057
NM_000260.4(MYO7A):c.783T>C (p.Gly261=) rs762667 0.50077
NM_000260.4(MYO7A):c.2905-162T>G rs59698916 0.48946
NM_000260.4(MYO7A):c.4755C>T (p.Ser1585=) rs7927472 0.47702
NM_000260.4(MYO7A):c.47T>C (p.Leu16Ser) rs1052030 0.47208
NM_000260.4(MYO7A):c.1080+65T>C rs4944145 0.46104
NM_000260.4(MYO7A):c.6439-31G>A rs883223 0.34445
NM_000260.4(MYO7A):c.6318G>A (p.Lys2106=) rs11237123 0.24897
NM_000260.4(MYO7A):c.4442-113A>G rs3781692 0.24810
NM_000260.4(MYO7A):c.133-88C>T rs12279716 0.19502
NM_000260.4(MYO7A):c.6558+16G>A rs883224 0.19125
NM_000260.4(MYO7A):c.736-47C>A rs3737454 0.11805
NM_000260.4(MYO7A):c.1004-35C>G rs2071151 0.09483
NM_000260.4(MYO7A):c.4441+148A>G rs4944149 0.05652
NM_000260.4(MYO7A):c.4441+195G>A rs4945157 0.03958
NM_000260.4(MYO7A):c.1343+8G>A rs2276278
NM_000260.4(MYO7A):c.1554+244T>C rs3740763
NM_000260.4(MYO7A):c.2695-58C>G rs3740762
NM_000260.4(MYO7A):c.3375+33G>C rs948972
NM_000260.4(MYO7A):c.3924+109G>A rs4944148
NM_000260.4(MYO7A):c.5860C>A (p.Leu1954Ile) rs948962

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