ClinVar Miner

List of variants in gene SRPX2 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014467.3(SRPX2):c.163+12T>C rs73555462 0.02331
NM_014467.3(SRPX2):c.460C>G (p.His154Asp) rs73636611 0.00298
NM_014467.3(SRPX2):c.1030C>A (p.Leu344Ile) rs149051060 0.00145
NM_014467.3(SRPX2):c.1373G>A (p.Arg458Gln) rs146051561 0.00133
NM_014467.3(SRPX2):c.840G>A (p.Ala280=) rs139377205 0.00118
NM_014467.3(SRPX2):c.660-16del rs764480482 0.00115
NM_014467.3(SRPX2):c.481C>A (p.Arg161=) rs150552508 0.00101
NM_014467.3(SRPX2):c.1293C>T (p.Tyr431=) rs138091242 0.00050
NM_014467.3(SRPX2):c.980A>G (p.Asn327Ser) rs121918363 0.00041
NM_014467.3(SRPX2):c.961+12C>T rs373436594 0.00031
NM_014467.3(SRPX2):c.693C>A (p.His231Gln) rs142719253 0.00022
NM_014467.3(SRPX2):c.1218-6C>T rs370981134 0.00019
NM_014467.3(SRPX2):c.449C>T (p.Ser150Phe) rs373847965 0.00019
NM_014467.3(SRPX2):c.624G>A (p.Pro208=) rs139514583 0.00018
NM_014467.3(SRPX2):c.893G>A (p.Arg298His) rs369663551 0.00011
NM_014467.3(SRPX2):c.248T>C (p.Leu83Pro) rs141168255 0.00007
NM_014467.3(SRPX2):c.962-16C>T rs190642591 0.00006
NM_014467.3(SRPX2):c.224A>T (p.Lys75Met) rs767072861 0.00005
NM_014467.3(SRPX2):c.542C>G (p.Pro181Arg) rs769478434 0.00004
NM_014467.3(SRPX2):c.671G>A (p.Arg224Gln) rs763624310 0.00003
NM_014467.3(SRPX2):c.-37A>G rs796053341 0.00002
NM_014467.3(SRPX2):c.1064G>A (p.Arg355Gln) rs541303724 0.00002
NM_014467.3(SRPX2):c.1229G>A (p.Arg410His) rs368571175 0.00002
NM_014467.3(SRPX2):c.961+1G>A rs1303998333 0.00002
NM_014467.3(SRPX2):c.1255G>A (p.Val419Met) rs797046012 0.00001
NM_014467.3(SRPX2):c.164T>C (p.Val55Ala) rs777972842 0.00001
NM_014467.3(SRPX2):c.646G>A (p.Gly216Ser) rs758845090 0.00001
NM_014467.3(SRPX2):c.1393G>A (p.Glu465Lys) rs898722174
NM_014467.3(SRPX2):c.355+1G>C
NM_014467.3(SRPX2):c.515G>A (p.Gly172Asp) rs775513104
NM_014467.3(SRPX2):c.605G>A (p.Arg202Gln) rs200784551
NM_014467.3(SRPX2):c.928C>T (p.Arg310Cys) rs758448998

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.