ClinVar Miner

List of variants reported as likely benign for parathyroid gland disorder by All of Us Research Program, National Institutes of Health

Included ClinVar conditions (50):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.762G>A (p.Leu254=) rs199909967 0.00018
NM_001370259.2(MEN1):c.1080C>T (p.Ile360=) rs147331514 0.00016
NM_001370259.2(MEN1):c.492C>T (p.Ala164=) rs146759807 0.00010
NM_001370259.2(MEN1):c.1003C>A (p.Arg335=) rs371364206 0.00006
NM_001370259.2(MEN1):c.1386C>A (p.Ala462=) rs771827808 0.00004
NM_001370259.2(MEN1):c.1401C>T (p.Ala467=) rs878855190 0.00004
NM_001370259.2(MEN1):c.1416C>T (p.Gly472=) rs764509990 0.00004
NM_001370259.2(MEN1):c.1800G>T (p.Leu600=) rs148825200 0.00004
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=) rs587780841 0.00003
NM_001370259.2(MEN1):c.471G>A (p.Val157=) rs878855194 0.00003
NM_001370259.2(MEN1):c.1155G>A (p.Ala385=) rs201091135 0.00002
NM_001370259.2(MEN1):c.115T>C (p.Leu39=) rs863224438 0.00002
NM_001370259.2(MEN1):c.639C>T (p.Ala213=) rs746067825 0.00002
NM_001370259.2(MEN1):c.1026G>A (p.Ala342=) rs878855184 0.00001
NM_001370259.2(MEN1):c.1287G>A (p.Thr429=) rs376598079 0.00001
NM_001370259.2(MEN1):c.1392G>A (p.Ala464=) rs754445482 0.00001
NM_001370259.2(MEN1):c.1395C>T (p.Ala465=) rs748820252 0.00001
NM_001370259.2(MEN1):c.1404G>A (p.Glu468=) rs755734265 0.00001
NM_001370259.2(MEN1):c.1482G>A (p.Pro494=) rs773363654 0.00001
NM_001370259.2(MEN1):c.1567G>A (p.Ala523Thr) rs760683615 0.00001
NM_001370259.2(MEN1):c.1578C>A (p.Ala526=) rs767655504 0.00001
NM_001370259.2(MEN1):c.1608G>A (p.Gln536=) rs1055457298 0.00001
NM_001370259.2(MEN1):c.1656T>C (p.Thr552=) rs143423552 0.00001
NM_001370259.2(MEN1):c.1758G>A (p.Gln586=) rs759563305 0.00001
NM_001370259.2(MEN1):c.219C>T (p.Gly73=) rs758434243 0.00001
NM_001370259.2(MEN1):c.258C>T (p.Ile86=) rs759731868 0.00001
NM_001370259.2(MEN1):c.303C>T (p.Val101=) rs1463347315 0.00001
NM_001370259.2(MEN1):c.336C>G (p.Val112=) rs1200092213 0.00001
NM_001370259.2(MEN1):c.345T>C (p.Arg115=) rs748948131 0.00001
NM_001370259.2(MEN1):c.446-11C>G rs1273035105 0.00001
NM_001370259.2(MEN1):c.513G>C (p.Arg171=) rs560870111 0.00001
NM_001370259.2(MEN1):c.570G>A (p.Gly190=) rs547249181 0.00001
NM_001370259.2(MEN1):c.609C>T (p.Asn203=) rs749844029 0.00001
NM_001370259.2(MEN1):c.681C>T (p.Tyr227=) rs778921501 0.00001
NM_001370259.2(MEN1):c.711G>A (p.Ala237=) rs144677807 0.00001
NM_001370259.2(MEN1):c.726C>T (p.Ala242=) rs1198651608 0.00001
NM_001370259.2(MEN1):c.843G>C (p.Gly281=) rs562620826 0.00001
NM_001370259.2(MEN1):c.856C>T (p.Leu286=) rs542321016 0.00001
NM_001370259.2(MEN1):c.861G>A (p.Glu287=) rs1336658836 0.00001
NM_001370259.2(MEN1):c.913-8C>T rs373893527 0.00001
NM_001370259.2(MEN1):c.*5C>G
NM_001370259.2(MEN1):c.-9C>G
NM_001370259.2(MEN1):c.102G>C (p.Leu34=) rs1255708093
NM_001370259.2(MEN1):c.1095T>C (p.Phe365=) rs1592640464
NM_001370259.2(MEN1):c.1119C>A (p.Pro373=) rs535417698
NM_001370259.2(MEN1):c.1170G>C (p.Pro390=) rs587780841
NM_001370259.2(MEN1):c.1186-10C>T rs762303621
NM_001370259.2(MEN1):c.1186-8del rs1555164452
NM_001370259.2(MEN1):c.1203T>C (p.Gly401=) rs878855187
NM_001370259.2(MEN1):c.1351-10A>G rs757569943
NM_001370259.2(MEN1):c.1377C>T (p.Ser459=) rs2136093597
NM_001370259.2(MEN1):c.1378C>A (p.Arg460=) rs104894267
NM_001370259.2(MEN1):c.1410G>A (p.Pro470=) rs1060503795
NM_001370259.2(MEN1):c.1569T>G (p.Ala523=) rs1592631415
NM_001370259.2(MEN1):c.15C>T (p.Ala5=)
NM_001370259.2(MEN1):c.1632A>G (p.Pro544=)
NM_001370259.2(MEN1):c.1677G>A (p.Lys559=) rs2136080688
NM_001370259.2(MEN1):c.1719C>T (p.Ser573=)
NM_001370259.2(MEN1):c.183C>T (p.Leu61=)
NM_001370259.2(MEN1):c.201C>T (p.Pro67=) rs1060503791
NM_001370259.2(MEN1):c.216T>G (p.Pro72=) rs1592659467
NM_001370259.2(MEN1):c.21G>A (p.Gln7=) rs1422628649
NM_001370259.2(MEN1):c.249G>C (p.Leu83=)
NM_001370259.2(MEN1):c.27G>A (p.Thr9=) rs1190267704
NM_001370259.2(MEN1):c.306C>T (p.Asp102=)
NM_001370259.2(MEN1):c.307C>T (p.Leu103=) rs1313314117
NM_001370259.2(MEN1):c.36G>A (p.Pro12=) rs775721366
NM_001370259.2(MEN1):c.441C>A (p.Ile147=)
NM_001370259.2(MEN1):c.446-10C>A rs1442401628
NM_001370259.2(MEN1):c.446-9C>A rs1371109251
NM_001370259.2(MEN1):c.591C>G (p.Thr197=) rs527294715
NM_001370259.2(MEN1):c.655-11C>T rs781234614
NM_001370259.2(MEN1):c.655-7C>T rs771297371
NM_001370259.2(MEN1):c.759G>T (p.Ser253=) rs201829546
NM_001370259.2(MEN1):c.784-8G>T rs766553550
NM_001370259.2(MEN1):c.79C>T (p.Leu27=) rs1006536599
NM_001370259.2(MEN1):c.825-10C>G rs999121619
NM_001370259.2(MEN1):c.837C>T (p.Ala279=) rs762092675
NM_001370259.2(MEN1):c.87A>C (p.Arg29=) rs1198070818
NM_001370259.2(MEN1):c.909C>T (p.His303=) rs878855200
NM_001370259.2(MEN1):c.913-11C>T rs2136122142
NM_001370259.2(MEN1):c.913-11_913-6dup
NM_001370259.2(MEN1):c.913-12A>C
NM_001370259.2(MEN1):c.913-13C>T rs1309344851
NM_001370259.2(MEN1):c.913-5T>C
NM_001370259.2(MEN1):c.915C>T (p.Gly305=)
NM_001370259.2(MEN1):c.936C>T (p.Tyr312=) rs386134260
NM_001370259.2(MEN1):c.942G>A (p.Arg314=)

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