ClinVar Miner

List of variants in gene XDH reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000379.4(XDH):c.3030T>C (p.Phe1010=) rs1884725 0.77423
NM_000379.4(XDH):c.3276+12A>G rs1366813 0.75380
NM_000379.4(XDH):c.3052-12C>G rs13415401 0.74590
NM_000379.4(XDH):c.2211C>T (p.Ile737=) rs2295475 0.24290
NM_000379.4(XDH):c.2107A>G (p.Ile703Val) rs17011368 0.05740
NM_000379.4(XDH):c.3717G>A (p.Glu1239=) rs207440 0.05236
NM_000379.4(XDH):c.3886C>T (p.Arg1296Trp) rs45564939 0.01229
NM_000379.4(XDH):c.1751A>C (p.Asp584Ala) rs45491693 0.00492
NM_000379.4(XDH):c.3271G>C (p.Val1091Leu) rs45619033 0.00328
NM_000379.4(XDH):c.2634T>C (p.Ile878=) rs146994573 0.00224
NM_000379.4(XDH):c.3536T>C (p.Ile1179Thr) rs139515054 0.00222
NM_000379.4(XDH):c.882C>T (p.Pro294=) rs138246330 0.00195
NM_000379.4(XDH):c.3875A>G (p.Lys1292Arg) rs73922346 0.00193
NM_000379.4(XDH):c.1726C>T (p.Arg576Trp) rs139772558 0.00170
NM_000379.4(XDH):c.636T>C (p.Phe212=) rs140225517 0.00095
NM_000379.4(XDH):c.2362A>T (p.Ile788Phe) rs141050887 0.00083
NM_000379.4(XDH):c.3018T>C (p.Phe1006=) rs144883930 0.00067
NM_000379.4(XDH):c.1911C>T (p.Ser637=) rs142197675 0.00058
NM_000379.4(XDH):c.2851G>A (p.Gly951Arg) rs142675390 0.00053
NM_000379.4(XDH):c.670C>T (p.Arg224Trp) rs147533056 0.00040
NM_000379.4(XDH):c.1773C>T (p.Ala591=) rs145108969 0.00023
NM_000379.4(XDH):c.1037C>T (p.Ala346Val) rs142388231 0.00022
NM_000379.4(XDH):c.2460C>T (p.Thr820=) rs143539472 0.00022
NM_000379.4(XDH):c.3920G>A (p.Arg1307His) rs138249576 0.00020
NM_000379.4(XDH):c.2794G>A (p.Ala932Thr) rs141291583 0.00018
NM_000379.4(XDH):c.1602C>T (p.Asp534=) rs61731080 0.00016
NM_000379.4(XDH):c.3249C>T (p.Ser1083=) rs45562835 0.00012
NM_000379.4(XDH):c.1856+10A>G rs372889724 0.00011
NM_000379.4(XDH):c.3789G>A (p.Pro1263=) rs202077714 0.00011
NM_000379.4(XDH):c.1990G>A (p.Val664Ile) rs201301387 0.00005
NM_000379.4(XDH):c.2013G>A (p.Val671=) rs200635805 0.00005
NM_000379.4(XDH):c.1041C>T (p.Ser347=) rs375950132
NM_000379.4(XDH):c.1494C>T (p.Pro498=)
NM_000379.4(XDH):c.159G>A (p.Val53=)
NM_000379.4(XDH):c.2022C>T (p.Asp674=)
NM_000379.4(XDH):c.339C>T (p.Cys113=)
NM_000379.4(XDH):c.3539T>C (p.Val1180Ala)
NM_000379.4(XDH):c.3764A>T (p.Tyr1255Phe)
NM_000379.4(XDH):c.3775-6G>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.