ClinVar Miner

List of variants in gene WNT5A reported as benign for not provided

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_003392.7(WNT5A):c.685-152T>C rs7622120 0.59201
NC_000003.12:g.55487689C>A rs620014 0.20470
NM_003392.7(WNT5A):c.684+290G>A rs3821658 0.20111
NM_003392.7(WNT5A):c.7-331G>A rs77344209 0.16236
NM_003392.7(WNT5A):c.140+47T>A rs73075443 0.14134
NM_003392.7(WNT5A):c.*1869C>T rs3732750 0.07148
NM_003392.7(WNT5A):c.391+11A>G rs6790979 0.00858
NM_003392.7(WNT5A):c.588C>T (p.Phe196=) rs200868061 0.00383
NM_003392.7(WNT5A):c.14T>C (p.Ile5Thr) rs200914260 0.00129
NM_003392.7(WNT5A):c.110C>G (p.Ala37Gly) rs190451046 0.00115
NM_003392.7(WNT5A):c.850T>C (p.Leu284=) rs375403509 0.00063
NM_003392.7(WNT5A):c.417C>T (p.Tyr139=) rs371576999 0.00030
NM_003392.7(WNT5A):c.807G>A (p.Lys269=) rs117338660 0.00016
NM_003392.7(WNT5A):c.502G>A (p.Ala168Thr) rs572796263 0.00009
NM_003392.7(WNT5A):c.20T>C (p.Ile7Thr) rs554762368 0.00006
NM_003392.7(WNT5A):c.937G>A (p.Glu313Lys) rs369701725 0.00003
NM_003392.7(WNT5A):c.456G>A (p.Arg152=) rs541491382 0.00001
NM_003392.7(WNT5A):c.822G>A (p.Ala274=) rs780501090 0.00001
NC_000003.12:g.55487931dup rs771387621
NM_003392.7(WNT5A):c.*1950_*1953dup rs78756487
NM_003392.7(WNT5A):c.*1952_*1953del rs78756487
NM_003392.7(WNT5A):c.*1953del rs78756487
NM_003392.7(WNT5A):c.*1953dup rs78756487
NM_003392.7(WNT5A):c.317A>G (p.Tyr106Cys)
NM_003392.7(WNT5A):c.405G>T (p.Thr135=) rs147104982
NM_003392.7(WNT5A):c.549C>T (p.Gly183=) rs2106916068
NM_003392.7(WNT5A):c.6+230A>C rs566926
NM_003392.7(WNT5A):c.661C>T (p.His221Tyr)
NM_003392.7(WNT5A):c.684+263C>T rs9818631
NM_003392.7(WNT5A):c.830G>A (p.Arg277Gln) rs369954366

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