ClinVar Miner

List of variants in gene WRN studied for not provided

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Total variants: 38
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HGVS dbSNP
GRCh37/hg19 8p12(chr8:30962693-30982426)x1
M117fs rs1563329555
NC_000008.11:g.31088887C>A
NC_000008.11:g.31100844del
NC_000008.11:g.31141606C>T
NM_000553.4(WRN):c.1530_1532delAGA (p.Glu510del) rs781777438
NM_000553.4(WRN):c.2067C>T (p.Ser689=) rs191757062
NM_000553.4(WRN):c.229G>C (p.Asp77His) rs144670883
NM_000553.4(WRN):c.2361G>T (p.Leu787=) rs1800392
NM_000553.4(WRN):c.2521G>A (p.Ala841Thr) rs748169173
NM_000553.4(WRN):c.2784A>G (p.Gly928=) rs755729832
NM_000553.4(WRN):c.2986G>A (p.Asp996Asn) rs138379977
NM_000553.4(WRN):c.3091G>C (p.Val1031Leu) rs138492730
NM_000553.4(WRN):c.3139-1G>C rs113993961
NM_000553.4(WRN):c.3222G>T (p.Leu1074Phe) rs1801195
NM_000553.4(WRN):c.3236C>T (p.Ser1079Leu) rs3087414
NM_000553.4(WRN):c.3383+5A>C rs374867947
NM_000553.4(WRN):c.3422C>T (p.Ser1141Leu) rs139323683
NM_000553.4(WRN):c.4083C>T (p.Ser1361=) rs1801196
NM_000553.4(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
NM_000553.4:c.1578delC rs780555196
NM_000553.5(WRN):c.1005A>T (p.Glu335Asp) rs770764781
NM_000553.5(WRN):c.107G>A (p.Arg36Gln) rs34084741
NM_000553.5(WRN):c.1161G>A (p.Met387Ile) rs1800391
NM_000553.5(WRN):c.1879G>A (p.Val627Ile) rs374688634
NM_000553.5(WRN):c.1909C>T (p.Arg637Trp) rs148286708
NM_000553.5(WRN):c.1992C>T (p.Leu664=) rs794727200
NM_000553.5(WRN):c.2900dup (p.Leu967Phefs) rs1554530901
NM_000553.5(WRN):c.3098G>T (p.Arg1033Leu) rs367789256
NM_000553.5(WRN):c.3453G>A (p.Glu1151=) rs144116311
NM_000553.5(WRN):c.355+4G>C rs145764920
NM_000553.5(WRN):c.3875C>A (p.Ser1292Tyr) rs142614369
NM_000553.5(WRN):c.4035G>A (p.Thr1345=) rs767115441
NM_000553.5(WRN):c.504+4A>G rs1563330043
NM_000553.5(WRN):c.513C>T (p.Cys171=) rs1800389
NM_000553.5(WRN):c.561A>G (p.Lys187=) rs775802030
NM_000553.5(WRN):c.747C>T (p.Asp249=) rs374142752
NM_000553.5(WRN):c.769A>G (p.Ile257Val) rs886044530

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