ClinVar Miner

List of variants in gene DSG2 reported as uncertain significance by Biesecker Lab/Clinical Genomics Section,National Institutes of Health

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Gene type:
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Total variants: 14
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HGVS dbSNP
NM_001943.5(DSG2):c.1063G>A (p.Ala355Thr) rs201046640
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn) rs370509593
NM_001943.5(DSG2):c.1346T>G (p.Leu449Arg) rs786205363
NM_001943.5(DSG2):c.1460T>C (p.Ile487Thr) rs776525113
NM_001943.5(DSG2):c.1478A>G (p.Asn493Ser) rs375679311
NM_001943.5(DSG2):c.1837G>A (p.Ala613Thr) rs368257724
NM_001943.5(DSG2):c.3040G>A (p.Val1014Ile) rs200830807
NM_001943.5(DSG2):c.3175T>A (p.Ser1059Thr) rs201786158
NM_001943.5(DSG2):c.3266G>T (p.Gly1089Val) rs200264407
NM_001943.5(DSG2):c.3293C>G (p.Ser1098Cys) rs2848673
NM_001943.5(DSG2):c.430G>A (p.Glu144Lys) rs199842209
NM_001943.5(DSG2):c.704A>G (p.Tyr235Cys) rs786205362
NM_001943.5(DSG2):c.841G>A (p.Val281Ile) rs201005720
NM_001943.5(DSG2):c.86T>C (p.Leu29Ser) rs786205361

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