ClinVar Miner

List of variants in gene DHCR24 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014762.4(DHCR24):c.*2555A>G rs657688 0.99941
NM_014762.4(DHCR24):c.1020+10A>G rs611057 0.99149
NM_014762.4(DHCR24):c.*1824T>G rs654561 0.98973
NM_014762.4(DHCR24):c.1026T>C (p.Ile342=) rs718265 0.66290
NM_014762.4(DHCR24):c.*1584T>C rs7374 0.40034
NM_014762.4(DHCR24):c.*2295G>C rs7373 0.39999
NM_014762.4(DHCR24):c.*221C>T rs1138030 0.19892
NM_014762.4(DHCR24):c.*324T>C rs74072036 0.08213
NM_014762.4(DHCR24):c.*1488C>T rs8990 0.07841
NM_014762.4(DHCR24):c.*788A>G rs9436941 0.03198
NM_014762.4(DHCR24):c.*462G>A rs648804 0.03193
NM_014762.4(DHCR24):c.*1965C>A rs11555500 0.02394
NM_014762.4(DHCR24):c.*1677T>C rs74496507 0.02139
NM_014762.4(DHCR24):c.180C>T (p.Leu60=) rs79857573 0.01223
NM_014762.4(DHCR24):c.*218C>A rs145558556 0.00942
NM_014762.4(DHCR24):c.360C>T (p.Asp120=) rs61733134 0.00798
NM_014762.4(DHCR24):c.1522G>A (p.Asp508Asn) rs11555496 0.00570
NM_014762.4(DHCR24):c.*1489G>A rs192013345 0.00558
NM_014762.4(DHCR24):c.*102C>T rs114267476 0.00523
NM_014762.4(DHCR24):c.*913C>T rs114343980 0.00451
NM_014762.4(DHCR24):c.*115C>T rs201545563 0.00378
NM_014762.4(DHCR24):c.*1424C>T rs113651566 0.00331
NM_014762.4(DHCR24):c.*2442G>T rs115017311 0.00323
NM_014762.4(DHCR24):c.81C>T (p.Leu27=) rs140995590 0.00294
NM_014762.4(DHCR24):c.*392C>T rs116490123 0.00293
NM_014762.4(DHCR24):c.1020+11G>A rs555618086 0.00258
NM_014762.4(DHCR24):c.-51G>T rs17552526 0.00243
NM_014762.4(DHCR24):c.*718G>A rs74072035 0.00232
NM_014762.4(DHCR24):c.*2084G>A rs74072034 0.00226
NM_014762.4(DHCR24):c.*914G>A rs140759061 0.00185
NM_014762.4(DHCR24):c.*2038G>A rs116411531 0.00162
NM_014762.4(DHCR24):c.*2200G>A rs558575804 0.00154
NM_014762.4(DHCR24):c.*2080C>T rs377656375 0.00148
NM_014762.4(DHCR24):c.*2554C>T rs144220338 0.00148
NM_014762.4(DHCR24):c.*1815A>T rs570922003 0.00147
NM_014762.4(DHCR24):c.616G>A (p.Glu206Lys) rs150688144 0.00092
NM_014762.4(DHCR24):c.*577C>T rs57714270 0.00065
NM_014762.4(DHCR24):c.*316T>G rs74072037 0.00063
NM_014762.4(DHCR24):c.*393G>A rs146650872 0.00057
NM_014762.4(DHCR24):c.*731T>C rs116289873 0.00056
NM_014762.4(DHCR24):c.*480C>T rs576670614 0.00054
NM_014762.4(DHCR24):c.731C>T (p.Pro244Leu) rs138667252 0.00048
NM_014762.4(DHCR24):c.639C>T (p.Ala213=) rs143779194 0.00044
NM_014762.4(DHCR24):c.-11G>A rs368314999 0.00041
NM_014762.4(DHCR24):c.-62G>A rs537895939 0.00039
NM_014762.4(DHCR24):c.*2394A>C rs548629632 0.00027
NM_014762.4(DHCR24):c.*653G>A rs372344030 0.00027
NM_014762.4(DHCR24):c.615C>T (p.Ser205=) rs147213053 0.00026
NM_014762.3(DHCR24):c.-77C>T rs548661780 0.00013
NM_014762.4(DHCR24):c.*944C>T rs79299252 0.00013
NM_014762.4(DHCR24):c.-42A>G rs371075692 0.00013
NM_014762.4(DHCR24):c.1329G>A (p.Pro443=) rs142984207 0.00013
NM_014762.4(DHCR24):c.*1881G>A rs757634950 0.00010
NM_014762.4(DHCR24):c.*27dup rs757256992 0.00010
NM_014762.4(DHCR24):c.*1264T>C rs553462271 0.00009
NM_014762.4(DHCR24):c.*1389T>C rs140078801 0.00009
NM_014762.4(DHCR24):c.*2119C>T rs886046414 0.00006
NM_014762.4(DHCR24):c.*42G>A rs200380515 0.00006
NM_014762.4(DHCR24):c.*1073C>G rs1044074687 0.00005
NM_014762.4(DHCR24):c.*1267G>A rs1175475634 0.00004
NM_014762.4(DHCR24):c.*278G>A rs772933580 0.00004
NM_014762.4(DHCR24):c.*676C>G rs762917924 0.00004
NM_014762.4(DHCR24):c.*984G>A rs776318516 0.00003
NM_014762.4(DHCR24):c.*172A>G rs886046420 0.00002
NM_014762.4(DHCR24):c.718C>T (p.Leu240=) rs191246223 0.00002
NM_014762.4(DHCR24):c.*125A>G rs914940982 0.00001
NM_014762.4(DHCR24):c.*1876T>C rs972764548 0.00001
NM_014762.4(DHCR24):c.*2468T>C rs1308283692 0.00001
NM_014762.4(DHCR24):c.*2503C>T rs886046412 0.00001
NM_014762.4(DHCR24):c.*2514A>G rs532882730 0.00001
NM_014762.4(DHCR24):c.1431C>T (p.Asn477=) rs1453549055 0.00001
NM_014762.4(DHCR24):c.712G>A (p.Val238Ile) rs886046421 0.00001
NM_014762.4(DHCR24):c.798C>T (p.Phe266=) rs142421002 0.00001
NM_014762.4(DHCR24):c.*1121A>G rs886046415
NM_014762.4(DHCR24):c.*1137G>C rs768244621
NM_014762.4(DHCR24):c.*1535G>A rs1646870155
NM_014762.4(DHCR24):c.*180_*181del rs886046419
NM_014762.4(DHCR24):c.*2081G>A rs373752257
NM_014762.4(DHCR24):c.*2245A>T rs886046413
NM_014762.4(DHCR24):c.*225T>C rs886046418
NM_014762.4(DHCR24):c.*426G>A rs1646876717
NM_014762.4(DHCR24):c.*434A>T rs886046417
NM_014762.4(DHCR24):c.*508T>C rs886046416
NM_014762.4(DHCR24):c.*597T>C rs1646875615
NM_014762.4(DHCR24):c.*600G>A rs184125615
NM_014762.4(DHCR24):c.-27G>C rs532827290
NM_014762.4(DHCR24):c.-27G>T rs532827290
NM_014762.4(DHCR24):c.1155G>A (p.Gln385=) rs1646893615
NM_014762.4(DHCR24):c.1228A>G (p.Ile410Val) rs1646890427
NM_014762.4(DHCR24):c.1397+2T>A rs1314761103
NM_014762.4(DHCR24):c.388-10G>T rs774425757
NM_014762.4(DHCR24):c.726C>A (p.Phe242Leu) rs138043637

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.