ClinVar Miner

List of variants in gene VWF reported as benign for not provided

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Gene type:
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Total variants: 129
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HGVS dbSNP gnomAD frequency
NM_000552.5(VWF):c.7771-173T>C rs216851 0.99629
NM_000552.5(VWF):c.220+52T>C rs6489694 0.99048
NM_000552.5(VWF):c.2282-133T>C rs216294 0.91760
NM_000552.5(VWF):c.2547-177A>C rs669667 0.91602
NM_000552.5(VWF):c.2547-172A>G rs499648 0.91599
NM_000552.5(VWF):c.2546+329T>C rs216324 0.91562
NM_000552.5(VWF):c.4641T>C (p.Thr1547=) rs216310 0.71518
NM_000552.5(VWF):c.4141A>G (p.Thr1381Ala) rs216311 0.71493
NM_000552.5(VWF):c.2546+25C>T rs216325 0.70354
NM_000552.5(VWF):c.7288-87T>C rs216855 0.68144
NM_000552.5(VWF):c.7548+188C>G rs2238110 0.67644
NM_000552.5(VWF):c.7548+170C>T rs11063965 0.67597
NM_000552.5(VWF):c.7548+231A>G rs10849365 0.66445
NM_000552.5(VWF):c.3675-75A>G rs216312 0.62640
NM_000552.5(VWF):c.56-319T>C rs1814250 0.62410
NM_000552.5(VWF):c.5665-118G>A rs216305 0.58621
NM_000552.5(VWF):c.6598+264C>T rs216898 0.57469
NM_000552.5(VWF):c.1433-173A>G rs2239158 0.56688
NM_000552.5(VWF):c.6598+198A>G rs76092459 0.55985
NM_000552.5(VWF):c.5843-111A>G rs216903 0.55941
NM_000552.3(VWF):c.-1303G>A rs7965413 0.53288
NM_000552.5(VWF):c.533-153del rs5796209 0.52751
NM_000552.5(VWF):c.6798+189G>A rs216896 0.51412
NM_000552.5(VWF):c.1451A>G (p.His484Arg) rs1800378 0.51348
NM_000552.5(VWF):c.6063+300C>T rs216901 0.51097
NM_000552.5(VWF):c.1-64C>T rs2286608 0.49101
NM_000552.5(VWF):c.1548T>C (p.Tyr516=) rs1800379 0.41956
NM_000552.5(VWF):c.2365A>G (p.Thr789Ala) rs1063856 0.40814
NM_000552.5(VWF):c.2385T>C (p.Tyr795=) rs1063857 0.40791
NM_000552.5(VWF):c.2282-121T>C rs1558519 0.40764
NM_000552.5(VWF):c.2282-122G>A rs1558520 0.40764
NM_000552.5(VWF):c.6598+200A>G rs78432670 0.30739
NM_000552.5(VWF):c.3222+31C>T rs73051263 0.29425
NM_000552.5(VWF):c.1946-226A>G rs73034900 0.26615
NM_000552.5(VWF):c.6976+129C>T rs24177 0.26574
NM_000552.5(VWF):c.2880G>A (p.Arg960=) rs1800380 0.25897
NM_000552.5(VWF):c.5053+130A>C rs17491418 0.24188
NM_000552.5(VWF):c.1182A>C (p.Ser394=) rs1800376 0.24101
NM_000552.5(VWF):c.1173A>T (p.Thr391=) rs1800375 0.23172
NM_000552.5(VWF):c.6598+213C>T rs216899 0.19827
NM_000552.5(VWF):c.998-27C>T rs55907031 0.16358
NM_000552.5(VWF):c.7287+127A>G rs216866 0.16311
NM_000552.5(VWF):c.6977-142C>T rs2192205 0.16251
NM_000552.5(VWF):c.954T>A (p.Asn318Lys) rs1800387 0.15296
NM_000552.5(VWF):c.1411G>A (p.Val471Ile) rs1800377 0.11338
NM_000552.5(VWF):c.657+11A>C rs7980045 0.10566
NM_000552.5(VWF):c.8253+32T>C rs2362483 0.10095
NM_000552.5(VWF):c.8253+39C>T rs2362482 0.10024
NM_000552.5(VWF):c.3240T>C (p.Tyr1080=) rs4021576 0.09832
NM_000552.5(VWF):c.3379+7A>C rs113446850 0.09700
NM_000552.5(VWF):c.4665A>C (p.Ala1555=) rs1800384 0.08554
NM_000552.5(VWF):c.4693G>T (p.Val1565Leu) rs1800385 0.08527
NM_000552.5(VWF):c.7288-19C>T rs3819540 0.08253
NM_000552.5(VWF):c.2555= (p.Gln852=) rs216321 0.08026
NM_000552.5(VWF):c.7081+298C>A rs2236774 0.07841
NM_000552.5(VWF):c.6064-225G>A rs12099542 0.07519
NM_000552.5(VWF):c.6063+25G>A rs3741906 0.07461
NM_000552.5(VWF):c.6799-106G>C rs11063974 0.07163
NM_000552.5(VWF):c.7287+60C>T rs2286937 0.07132
NM_000552.5(VWF):c.7288-21C>T rs3819539 0.07127
NM_000552.5(VWF):c.7081+281G>A rs2236773 0.07125
NM_000552.5(VWF):c.6976+59C>T rs2070885 0.07075
NM_000552.5(VWF):c.6976+259A>G rs2070887 0.07070
NM_000552.5(VWF):c.6598+121C>T rs10849376 0.07056
NM_000552.5(VWF):c.6902-210G>C rs2070883 0.07049
NM_000552.5(VWF):c.6902-105G>A rs2070884 0.07043
NM_000552.5(VWF):c.3579T>C (p.Pro1193=) rs16933969 0.06947
NM_000552.5(VWF):c.1626G>A (p.Ala542=) rs35365059 0.06825
NM_000552.5(VWF):c.6598+126G>A rs216900 0.06581
NM_000552.5(VWF):c.6554G>A (p.Arg2185Gln) rs2229446 0.06069
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.2220G>A (p.Met740Ile) rs2228317 0.05696
NM_000552.5(VWF):c.1945+24C>T rs61908661 0.04957
NM_000552.5(VWF):c.3258C>T (p.Tyr1086=) rs112634786 0.04897
NM_000552.5(VWF):c.3414C>T (p.Asn1138=) rs560397436 0.04853
NM_000552.5(VWF):c.6345T>A (p.Thr2115=) rs11537642 0.04599
NM_000552.5(VWF):c.7682T>A (p.Phe2561Tyr) rs35335161 0.04046
NM_000552.5(VWF):c.3795G>A (p.Pro1265=) rs2228319 0.03767
NM_000552.5(VWF):c.4138A>G (p.Ile1380Val) rs11063988 0.03649
NM_000552.5(VWF):c.2451T>A (p.His817Gln) rs57950734 0.03591
NM_000552.5(VWF):c.4304A>G (p.Asn1435Ser) rs11063987 0.03448
NM_000552.5(VWF):c.7997C>T (p.Thr2666Met) rs78353028 0.02215
NM_000552.5(VWF):c.1794C>T (p.Ala598=) rs35302737 0.02100
NM_000552.5(VWF):c.3379+13G>A rs2885752 0.01966
NM_000552.5(VWF):c.1433-10T>C rs66722092 0.01853
NM_000552.5(VWF):c.5667C>T (p.Pro1889=) rs56981471 0.01850
NM_000552.5(VWF):c.6902-5T>A rs112046757 0.01517
NM_000552.5(VWF):c.6532G>T (p.Ala2178Ser) rs34230288 0.01330
NM_000552.5(VWF):c.5843-8C>G rs34444862 0.01303
NM_000552.5(VWF):c.390C>T (p.Ser130=) rs2229444 0.01260
NM_000552.5(VWF):c.2771G>A (p.Arg924Gln) rs33978901 0.01237
NM_000552.5(VWF):c.7698G>A (p.Lys2566=) rs16932285 0.00947
NM_000552.5(VWF):c.5313G>T (p.Gly1771=) rs2229448 0.00914
NM_000552.5(VWF):c.4196G>A (p.Arg1399His) rs1800382 0.00907
NM_000552.5(VWF):c.2900G>A (p.Gly967Asp) rs141087261 0.00842
NM_000552.5(VWF):c.5277C>T (p.Asp1759=) rs41276736 0.00826
NM_000552.5(VWF):c.7887+12T>C rs55687637 0.00814
NM_000552.5(VWF):c.5173C>T (p.Pro1725Ser) rs78302129 0.00774
NM_000552.5(VWF):c.2510C>A (p.Ala837Asp) rs75645183 0.00739
NM_000552.5(VWF):c.5515T>C (p.Leu1839=) rs141134620 0.00734
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.5053+37G>A rs35122657 0.00633
NM_000552.5(VWF):c.7771-10C>T rs189370859 0.00565
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.3789G>A (p.Ser1263=) rs199831474 0.00146
NM_000552.5(VWF):c.1329C>T (p.Ser443=) rs142404899 0.00058
NM_000552.5(VWF):c.7362C>T (p.Thr2454=) rs146504585 0.00038
GRCh37/hg19 12p13.31(chr12:6232426-6246446)x1
NM_000552.5(VWF):c.1433-128G>T rs2239159
NM_000552.5(VWF):c.1945+209G>C rs73036509
NM_000552.5(VWF):c.1946-17_1946-15dup rs10622288
NM_000552.5(VWF):c.2282-42C>A rs216293
NM_000552.5(VWF):c.2443-291C>T rs216326
NM_000552.5(VWF):c.2967+243dup rs71445694
NM_000552.5(VWF):c.3101_3103del (p.Thr1034del) rs368366214
NM_000552.5(VWF):c.3485_3486inv (p.Pro1162Leu)
NM_000552.5(VWF):c.3692A>C (p.Asn1231Thr) rs61749368
NM_000552.5(VWF):c.4414G>C (p.Asp1472His) rs1800383
NM_000552.5(VWF):c.4824C>T (p.Thr1608=) rs142635883
NM_000552.5(VWF):c.5053+303_5053+304del rs67479635
NM_000552.5(VWF):c.5053+304del rs67479635
NM_000552.5(VWF):c.6976+146G>A rs2070886
NM_000552.5(VWF):c.6977-225TATC[3] rs10535241
NM_000552.5(VWF):c.7437+86dup rs5796198
NM_000552.5(VWF):c.7549-59A>C rs2270239
NM_000552.5(VWF):c.7888-17T>C

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