ClinVar Miner

List of variants in gene GRN studied for not specified

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002087.4(GRN):c.835+7G>A rs72824736 0.04753
NM_002087.4(GRN):c.384T>C (p.Asp128=) rs25646 0.02616
NM_002087.4(GRN):c.55C>T (p.Arg19Trp) rs63750723 0.01303
NM_002087.4(GRN):c.1544G>C (p.Gly515Ala) rs25647 0.00781
NM_002087.3(GRN):c.-72G>T rs76783532 0.00635
NM_002087.4(GRN):c.264+7G>A rs60100877 0.00548
NM_002087.4(GRN):c.1227G>A (p.Thr409=) rs140298583 0.00326
NM_002087.4(GRN):c.1298G>A (p.Arg433Gln) rs114248177 0.00247
NM_002087.4(GRN):c.970G>A (p.Ala324Thr) rs63750541 0.00112
NM_002087.3(GRN):c.-45C>G rs563336550 0.00057
NM_002087.4(GRN):c.393C>G (p.Phe131Leu) rs149180605 0.00052
NM_002087.4(GRN):c.903G>A (p.Ser301=) rs63750142 0.00044
NM_002087.3(GRN):c.-56T>G rs909307115 0.00032
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln) rs63751100 0.00022
NM_002087.4(GRN):c.229G>A (p.Val77Ile) rs148531161 0.00008
NM_002087.4(GRN):c.1742A>T (p.Asp581Val) rs768223928 0.00007
NM_002087.4(GRN):c.1641C>T (p.Arg547=) rs149658268 0.00006
NM_002087.4(GRN):c.1486G>A (p.Glu496Lys) rs764615963 0.00001
NM_002087.4(GRN):c.473G>A (p.Cys158Tyr) rs63750163 0.00001
NM_002087.4(GRN):c.620T>C (p.Met207Thr) rs776198499 0.00001
NM_002087.4(GRN):c.1672_1673delinsGA (p.Cys558Asp) rs2143350279
NM_002087.4(GRN):c.99C>T (p.Asp33=) rs63750742
NM_002087.4:c.(?_-41)_(-8+1_-7-1)del

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