ClinVar Miner

List of variants reported as likely benign by Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington

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Total variants: 16
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 12q24.33(chr12:129802877-130479794)x3
GRCh37/hg19 13q12.12(chr13:23515553-24927971)x1
GRCh37/hg19 13q31.3(chr13:92520462-92715040)x1
GRCh37/hg19 15q12(chr15:25774319-26266785)x3
GRCh37/hg19 15q21.3(chr15:57350251-58025960)x3
GRCh37/hg19 16p13.11-12.3(chr16:16633361-17879988)x3
GRCh37/hg19 19p12(chr19:22208751-23199700)x3
GRCh37/hg19 1p31.1(chr1:74129905-74702475)x3
GRCh37/hg19 1q43(chr1:242292690-243094146)x4
GRCh37/hg19 21q22.11-22.12(chr21:35733290-35904053)x3
GRCh37/hg19 2q22.1-22.2(chr2:141632103-142270676)x1
GRCh37/hg19 3p14.2(chr3:59709050-61021526)x3
GRCh37/hg19 3p26.3-26.2(chr3:2152370-2806287)x1
GRCh37/hg19 4q13.1(chr4:60902170-61825240)x1
GRCh37/hg19 Xp22.31(chrX:7906287-8432715)x2
GRCh37/hg19 Xp22.33(chrX:892049-1425973)x3

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