ClinVar Miner

List of variants in gene CSF1R reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 116
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001288705.3(CSF1R):c.*36A>C rs2066934 0.82488
NM_001288705.3(CSF1R):c.*35C>T rs2066933 0.82461
NM_001288705.3(CSF1R):c.84T>C (p.Pro28=) rs216123 0.46517
NM_001288705.3(CSF1R):c.*769A>G rs3828609 0.16291
NM_001288705.3(CSF1R):c.1626+7C>T rs34928010 0.13020
NM_001288705.3(CSF1R):c.*310C>A rs41497048 0.10361
NM_001288705.3(CSF1R):c.*512T>C rs13117 0.09042
NM_001288705.3(CSF1R):c.1085A>G (p.His362Arg) rs10079250 0.08472
NM_001288705.3(CSF1R):c.*234del rs376905470 0.03884
NM_001288705.3(CSF1R):c.294C>T (p.His98=) rs17652007 0.03331
NM_001288705.3(CSF1R):c.2535C>G (p.Leu845=) rs56327604 0.03157
NM_001288705.3(CSF1R):c.733G>T (p.Ala245Ser) rs41338945 0.02627
NM_001288705.3(CSF1R):c.1626+12C>T rs116168767 0.01490
NM_001288705.3(CSF1R):c.1083-8T>C rs41428145 0.01068
NM_001288705.3(CSF1R):c.1237G>A (p.Gly413Ser) rs34951517 0.00996
NM_001288705.3(CSF1R):c.2709C>T (p.Phe903=) rs41287094 0.00742
NM_001288705.3(CSF1R):c.*604A>G rs150244467 0.00631
NM_001288705.3(CSF1R):c.282C>T (p.Ser94=) rs41287102 0.00495
NM_001288705.3(CSF1R):c.*405G>C rs1058920 0.00386
NM_001288705.3(CSF1R):c.2760G>C (p.Glu920Asp) rs34030164 0.00332
NM_001288705.3(CSF1R):c.95T>G (p.Val32Gly) rs56048668 0.00332
NM_001288705.3(CSF1R):c.1552G>A (p.Val518Met) rs138432536 0.00329
NM_001288705.3(CSF1R):c.*64C>T rs144642625 0.00270
NM_001288705.3(CSF1R):c.2799T>C (p.Gly933=) rs41287092 0.00258
NM_001288705.3(CSF1R):c.268C>A (p.Pro90Thr) rs150475750 0.00198
NM_001288705.3(CSF1R):c.2862C>T (p.Cys954=) rs56005231 0.00146
NM_001288705.3(CSF1R):c.1626+3G>A rs41424145 0.00137
NM_001288705.3(CSF1R):c.802G>A (p.Val268Ile) rs143274491 0.00107
NM_001288705.3(CSF1R):c.*531C>T rs367836988 0.00104
NM_001288705.3(CSF1R):c.2805C>T (p.Ser935=) rs147476583 0.00102
NM_001288705.3(CSF1R):c.835G>A (p.Val279Met) rs3829986 0.00089
NM_001288705.3(CSF1R):c.764A>T (p.Asn255Ile) rs146406037 0.00086
NM_001288705.3(CSF1R):c.192C>T (p.Gly64=) rs56282370 0.00081
NM_001288705.3(CSF1R):c.881G>A (p.Arg294Gln) rs149168939 0.00067
NM_001288705.3(CSF1R):c.*774A>G rs371174880 0.00058
NM_001288705.3(CSF1R):c.178C>T (p.Leu60=) rs55865465 0.00048
NM_001288705.3(CSF1R):c.316C>T (p.Arg106Trp) rs143025739 0.00046
NM_001288705.3(CSF1R):c.2746G>A (p.Glu916Lys) rs142435467 0.00033
NM_001288705.3(CSF1R):c.*715C>T rs572860735 0.00027
NM_001288705.3(CSF1R):c.*532G>A rs527300272 0.00024
NM_001288705.3(CSF1R):c.593-9C>T rs191671408 0.00023
NM_001288705.3(CSF1R):c.1716C>T (p.Asn572=) rs772750557 0.00017
NM_001288705.3(CSF1R):c.1404G>A (p.Val468=) rs201654254 0.00016
NM_001288705.3(CSF1R):c.1929C>T (p.His643=) rs184499252 0.00015
NM_001288705.3(CSF1R):c.1701G>A (p.Thr567=) rs567201624 0.00014
NM_001288705.3(CSF1R):c.2508C>T (p.Ser836=) rs146691087 0.00013
NM_001288705.3(CSF1R):c.895G>A (p.Ala299Thr) rs370361925 0.00011
NM_001288705.3(CSF1R):c.2761C>T (p.Arg921Trp) rs202216061 0.00010
NM_001288705.3(CSF1R):c.*116C>T rs188032016 0.00007
NM_001288705.3(CSF1R):c.*249A>G rs543512013 0.00007
NM_001288705.3(CSF1R):c.1111C>T (p.Leu371=) rs556530627 0.00006
NM_001288705.3(CSF1R):c.1520C>T (p.Thr507Met) rs538359948 0.00006
NM_001288705.3(CSF1R):c.2129G>A (p.Arg710His) rs201569135 0.00006
NM_001288705.3(CSF1R):c.2166C>T (p.Thr722=) rs376570011 0.00006
NM_001288705.3(CSF1R):c.2603T>G (p.Leu868Arg) rs281860278 0.00006
NM_001288705.3(CSF1R):c.1216G>A (p.Val406Ile) rs377213618 0.00005
NM_001288705.3(CSF1R):c.224C>T (p.Thr75Ile) rs748096324 0.00005
NM_001288705.3(CSF1R):c.*199A>G rs138239430 0.00004
NM_001288705.3(CSF1R):c.1606C>G (p.Leu536Val) rs55942044 0.00004
NM_001288705.3(CSF1R):c.2499G>A (p.Thr833=) rs149872699 0.00004
NM_001288705.3(CSF1R):c.2886C>T (p.Pro962=) rs370648666 0.00004
NM_001288705.3(CSF1R):c.943G>A (p.Val315Met) rs756763314 0.00004
NM_001288705.3(CSF1R):c.1560C>T (p.Val520=) rs767351282 0.00003
NM_001288705.3(CSF1R):c.*221C>T rs574587482 0.00002
NM_001288705.3(CSF1R):c.*500C>T rs138905856 0.00002
NM_001288705.3(CSF1R):c.*721_*724del rs543445510 0.00002
NM_001288705.3(CSF1R):c.2165C>A (p.Thr722Asn) rs371017407 0.00002
NM_001288705.3(CSF1R):c.2258G>A (p.Arg753Gln) rs560352241 0.00002
NM_001288705.3(CSF1R):c.2763+7G>A rs371729310 0.00002
NM_001288705.3(CSF1R):c.449G>A (p.Arg150His) rs1029057991 0.00002
NM_001288705.3(CSF1R):c.518A>G (p.Gln173Arg) rs780547939 0.00002
NM_001288705.3(CSF1R):c.*101T>C rs1757050261 0.00001
NM_001288705.3(CSF1R):c.*733G>A rs1263927433 0.00001
NM_001288705.3(CSF1R):c.1179G>A (p.Thr393=) rs767546915 0.00001
NM_001288705.3(CSF1R):c.1220T>C (p.Ile407Thr) rs372924085 0.00001
NM_001288705.3(CSF1R):c.1319+12C>T rs374820982 0.00001
NM_001288705.3(CSF1R):c.1518C>T (p.His506=) rs1757872206 0.00001
NM_001288705.3(CSF1R):c.1587G>A (p.Leu529=) rs776636931 0.00001
NM_001288705.3(CSF1R):c.1728G>A (p.Glu576=) rs549280708 0.00001
NM_001288705.3(CSF1R):c.2622A>C (p.Gln874His) rs886060255 0.00001
NM_001288705.3(CSF1R):c.2654+12G>T rs1252952936 0.00001
NM_001288705.3(CSF1R):c.2796C>T (p.Ser932=) rs778420941 0.00001
NM_001288705.3(CSF1R):c.354C>T (p.Phe118=) rs750046493 0.00001
NM_001288705.3(CSF1R):c.*156G>A rs886060254
NM_001288705.3(CSF1R):c.*230C>A rs373205661
NM_001288705.3(CSF1R):c.*231C>G rs78449650
NM_001288705.3(CSF1R):c.*231_*232insG rs3216780
NM_001288705.3(CSF1R):c.*232C>G rs952163871
NM_001288705.3(CSF1R):c.*232_*233dup rs200927456
NM_001288705.3(CSF1R):c.*233C>A rs1034592507
NM_001288705.3(CSF1R):c.*263G>C rs1031187832
NM_001288705.3(CSF1R):c.*530C>A rs1046339426
NM_001288705.3(CSF1R):c.*539C>A rs373206666
NM_001288705.3(CSF1R):c.*561C>T rs886060253
NM_001288705.3(CSF1R):c.*56G>A rs745652939
NM_001288705.3(CSF1R):c.*5T>C rs894716510
NM_001288705.3(CSF1R):c.*619G>T rs1757015333
NM_001288705.3(CSF1R):c.*749C>T rs564262683
NM_001288705.3(CSF1R):c.*768T>G rs1757001567
NM_001288705.3(CSF1R):c.1306G>A (p.Gly436Ser) rs886060257
NM_001288705.3(CSF1R):c.1510+13C>G rs533789269
NM_001288705.3(CSF1R):c.1753+15C>T rs886060256
NM_001288705.3(CSF1R):c.195C>T (p.Ser65=) rs1758508357
NM_001288705.3(CSF1R):c.2132+5C>T rs17110908
NM_001288705.3(CSF1R):c.2132+8del rs776168370
NM_001288705.3(CSF1R):c.2136C>T (p.Asp712=) rs772656669
NM_001288705.3(CSF1R):c.2217G>T (p.Glu739Asp) rs199915312
NM_001288705.3(CSF1R):c.2239G>A (p.Gly747Arg) rs41355444
NM_001288705.3(CSF1R):c.225C>T (p.Thr75=) rs781021919
NM_001288705.3(CSF1R):c.2345G>A (p.Arg782His) rs281860281
NM_001288705.3(CSF1R):c.2762G>C (p.Arg921Pro) rs56059682
NM_001288705.3(CSF1R):c.299A>G (p.Tyr100Cys) rs1413974974
NM_001288705.3(CSF1R):c.307+5G>A rs886060258
NM_001288705.3(CSF1R):c.337C>G (p.Gln113Glu) rs1758477235
NM_001288705.3(CSF1R):c.497G>A (p.Arg166Lys) rs1187678502
NM_001288705.3(CSF1R):c.733G>A (p.Ala245Thr) rs41338945

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.