ClinVar Miner

List of variants in gene VWF reported as likely benign for not specified

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000552.5(VWF):c.3426T>C (p.Cys1142=) rs535693463 0.05771
NM_000552.5(VWF):c.3486A>G (p.Pro1162=) rs546732699 0.05708
NM_000552.5(VWF):c.3485C>T (p.Pro1162Leu) rs566672558 0.05671
NM_000552.5(VWF):c.2900G>A (p.Gly967Asp) rs141087261 0.00842
NM_000552.5(VWF):c.3686T>G (p.Val1229Gly) rs61749367 0.00656
NM_000552.5(VWF):c.391G>A (p.Gly131Ser) rs76505074 0.00651
NM_000552.5(VWF):c.55+8C>A rs114713980 0.00452
NM_000552.5(VWF):c.6187C>T (p.Pro2063Ser) rs61750615 0.00437
NM_000552.5(VWF):c.5170+10C>T rs61750601 0.00400
NM_000552.5(VWF):c.4457C>T (p.Ser1486Leu) rs149424724 0.00282
NM_000552.5(VWF):c.114C>T (p.Phe38=) rs2229443 0.00241
NM_000552.5(VWF):c.7059G>C (p.Glu2353Asp) rs112319661 0.00195
NM_000552.5(VWF):c.6099C>T (p.Tyr2033=) rs55784921 0.00132
NM_000552.5(VWF):c.6303C>A (p.Gly2101=) rs115914543 0.00132
NM_000552.5(VWF):c.546G>A (p.Ser182=) rs143054357 0.00125
NM_000552.5(VWF):c.8289C>T (p.Asp2763=) rs149309674 0.00116
NM_000552.5(VWF):c.1563C>T (p.Cys521=) rs575601321 0.00114
NM_000552.5(VWF):c.6756G>A (p.Glu2252=) rs71581020 0.00110
NM_000552.5(VWF):c.2586G>T (p.Val862=) rs34510401 0.00109
NM_000552.5(VWF):c.7082-13G>C rs71581025 0.00108
NM_000552.5(VWF):c.2739A>C (p.Gly913=) rs35191786 0.00102
NM_000552.5(VWF):c.5312-19A>C rs200237834 0.00098
NM_000552.5(VWF):c.1329C>T (p.Ser443=) rs142404899 0.00058
NM_000552.5(VWF):c.4146G>T (p.Leu1382=) rs140464171 0.00044
NM_000552.5(VWF):c.1107C>G (p.Thr369=) rs149640698 0.00042
NM_000552.5(VWF):c.858C>T (p.Thr286=) rs776206258 0.00011
NM_000552.5(VWF):c.1533+15G>A rs184217564 0.00010
NM_000552.5(VWF):c.6069G>A (p.Thr2023=) rs375810839 0.00009
NM_000552.5(VWF):c.5073C>T (p.Asp1691=) rs549367616 0.00004
NM_000552.5(VWF):c.2025G>A (p.Pro675=) rs779045480 0.00003
NM_000552.5(VWF):c.3379+10G>A rs377317762 0.00003
NM_000552.5(VWF):c.3747T>C (p.Asp1249=) rs200893595 0.00003
NM_000552.5(VWF):c.4011G>A (p.Pro1337=) rs1800381 0.00002
NM_000552.5(VWF):c.4800G>A (p.Ala1600=) rs201264909 0.00002
NM_000552.5(VWF):c.1869C>T (p.Cys623=) rs61754017 0.00001
NM_000552.5(VWF):c.6599-5dup rs768221292 0.00001
NM_000552.5(VWF):c.1110-6dup rs534403271
NM_000552.5(VWF):c.1613C>T (p.Pro538Leu) rs139196998
NM_000552.5(VWF):c.1848G>C (p.Ser616=)
NM_000552.5(VWF):c.1946-9C>T
NM_000552.5(VWF):c.2187-30G>C rs1591882446
NM_000552.5(VWF):c.2694C>T (p.Cys898=)
NM_000552.5(VWF):c.2973A>G (p.Lys991=)
NM_000552.5(VWF):c.3024C>T (p.Thr1008=)
NM_000552.5(VWF):c.3692A>C (p.Asn1231Thr) rs61749368
NM_000552.5(VWF):c.56-17G>A
NM_000552.5(VWF):c.5793G>A (p.Gln1931=)
NM_000552.5(VWF):c.6104G>A (p.Gly2035Asp)
NM_000552.5(VWF):c.6901+14C>T
NM_000552.5(VWF):c.7624A>G (p.Ile2542Val)
NM_000552.5(VWF):c.7782T>A (p.Thr2594=) rs886038359

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