ClinVar Miner

List of variants reported as likely benign for Chuvash polycythemia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 88
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HGVS dbSNP
NM_000551.3(VHL):c.105C>G (p.Ala35=) rs1310829877
NM_000551.3(VHL):c.108G>A (p.Glu36=) rs1553619344
NM_000551.3(VHL):c.114C>T (p.Ser38=) rs417164
NM_000551.3(VHL):c.115G>C (p.Gly39Arg) rs768650092
NM_000551.3(VHL):c.119C>T (p.Pro40Leu) rs200343185
NM_000551.3(VHL):c.12G>A (p.Arg4=) rs1553619274
NM_000551.3(VHL):c.134C>G (p.Pro45Arg) rs199583685
NM_000551.3(VHL):c.135G>A (p.Pro45=) rs773519476
NM_000551.3(VHL):c.150C>A (p.Ala50=) rs61751580
NM_000551.3(VHL):c.159G>A (p.Glu53=) rs1553619385
NM_000551.3(VHL):c.165G>A (p.Glu55=) rs1553619391
NM_000551.3(VHL):c.168C>T (p.Ala56=) rs864622714
NM_000551.3(VHL):c.172C>A (p.Arg58=) rs757781272
NM_000551.3(VHL):c.192C>T (p.Arg64=) rs1012545817
NM_000551.3(VHL):c.195G>C (p.Ser65=) rs1553619409
NM_000551.3(VHL):c.213C>T (p.Pro71=) rs201663073
NM_000551.3(VHL):c.216C>T (p.Ser72=) rs774557051
NM_000551.3(VHL):c.21C>T (p.Asn7=) rs1060503561
NM_000551.3(VHL):c.225C>T (p.Ile75=) rs768104793
NM_000551.3(VHL):c.240T>C (p.Ser80=) rs1553619424
NM_000551.3(VHL):c.246C>T (p.Arg82=) rs587780993
NM_000551.3(VHL):c.249C>G (p.Val83=) rs1271292937
NM_000551.3(VHL):c.255G>A (p.Leu85=) rs876658508
NM_000551.3(VHL):c.255G>T (p.Leu85=) rs876658508
NM_000551.3(VHL):c.267C>T (p.Leu89=) rs755794553
NM_000551.3(VHL):c.276C>T (p.Asp92=) rs1442093467
NM_000551.3(VHL):c.27C>T (p.Asp9=) rs1017141110
NM_000551.3(VHL):c.285G>T (p.Pro95=) rs975432073
NM_000551.3(VHL):c.291C>G (p.Pro97=) rs1805159
NM_000551.3(VHL):c.297A>C (p.Pro99=) rs774753107
NM_000551.3(VHL):c.315G>C (p.Thr105=) rs769102979
NM_000551.3(VHL):c.324C>T (p.Arg108=) rs878854124
NM_000551.3(VHL):c.340+7G>C rs869025635
NM_000551.3(VHL):c.340+8C>A rs756068442
NM_000551.3(VHL):c.341-10G>C rs140064807
NM_000551.3(VHL):c.341-5G>A rs372340900
NM_000551.3(VHL):c.341-6C>T rs191201783
NM_000551.3(VHL):c.345C>T (p.His115=) rs864622646
NM_000551.3(VHL):c.366A>G (p.Ala122=) rs1474241640
NM_000551.3(VHL):c.375C>T (p.His125=) rs863224372
NM_000551.3(VHL):c.385C>T (p.Leu129=) rs369018004
NM_000551.3(VHL):c.387G>T (p.Leu129=) rs778846471
NM_000551.3(VHL):c.402A>G (p.Glu134=) rs201482330
NM_000551.3(VHL):c.411G>C (p.Val137=) rs1553619969
NM_000551.3(VHL):c.420C>A (p.Leu140=) rs369465430
NM_000551.3(VHL):c.45G>A (p.Ala15=) rs563813895
NM_000551.3(VHL):c.463+9G>A rs1057522720
NM_000551.3(VHL):c.464-10G>A rs552930903
NM_000551.3(VHL):c.48G>A (p.Glu16=) rs1057522140
NM_000551.3(VHL):c.504C>T (p.Ser168=) rs1553620323
NM_000551.3(VHL):c.507A>C (p.Leu169=) rs878854126
NM_000551.3(VHL):c.540C>T (p.Ile180=) rs374927292
NM_000551.3(VHL):c.549G>A (p.Ser183=) rs193922614
NM_000551.3(VHL):c.54A>C (p.Ala18=) rs1305687580
NM_000551.3(VHL):c.552C>T (p.Leu184=) rs779157605
NM_000551.3(VHL):c.555C>T (p.Tyr185=) rs864622109
NM_000551.3(VHL):c.561T>C (p.Asp187=) rs370769257
NM_000551.3(VHL):c.579T>C (p.Asn193=) rs1060503558
NM_000551.3(VHL):c.57C>A (p.Gly19=) rs1453582828
NM_000551.3(VHL):c.60C>G (p.Val20=) rs1553619311
NM_000551.3(VHL):c.612G>A (p.Glu204=) rs747805018
NM_000551.3(VHL):c.639T>C (p.Asp213=) rs775624944
NM_000551.3(VHL):c.6C>G (p.Pro2=) rs1014417508
NM_000551.3(VHL):c.72C>A (p.Gly24=) rs1375079282
NM_000551.3(VHL):c.75T>C (p.Pro25=) rs1553619317
NM_000551.3(VHL):c.99G>C (p.Ser33=) rs912159589
NM_000551.4(VHL):c.120G>A (p.Pro40=) rs1189123803
NM_000551.4(VHL):c.141A>G (p.Glu47=) rs1353920298
NM_000551.4(VHL):c.222C>G (p.Val74=) rs759737367
NM_000551.4(VHL):c.237C>G (p.Arg79=) rs760899424
NM_000551.4(VHL):c.252G>C (p.Val84=) rs1436342215
NM_000551.4(VHL):c.258C>T (p.Pro86=) rs781063331
NM_000551.4(VHL):c.261A>G (p.Val87=) rs1386184754
NM_000551.4(VHL):c.267C>A (p.Leu89=) rs755794553
NM_000551.4(VHL):c.294C>T (p.Tyr98=) rs1559426115
NM_000551.4(VHL):c.340+10C>A rs777622214
NM_000551.4(VHL):c.340+10C>T rs777622214
NM_000551.4(VHL):c.340+701G>A
NM_000551.4(VHL):c.340+809A>G
NM_000551.4(VHL):c.39A>G (p.Val13=) rs996469746
NM_000551.4(VHL):c.420C>T (p.Leu140=) rs369465430
NM_000551.4(VHL):c.474G>T (p.Leu158=) rs1575932005
NM_000551.4(VHL):c.489C>G (p.Leu163=) rs1575932067
NM_000551.4(VHL):c.525C>T (p.Tyr175=) rs5030835
NM_000551.4(VHL):c.531A>G (p.Arg177=) rs766088261
NM_000551.4(VHL):c.594G>C (p.Leu198=) rs1575932599
NM_000551.4(VHL):c.606A>G (p.Thr202=) rs1575932637
NM_000551.4(VHL):c.69C>T (p.Tyr23=) rs1553619313

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