List of variants in gene ZFPM2 reported as benign for cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_012082.4(ZFPM2):c.302-13C>T	rs3735953	0.68152
NM_012082.4(ZFPM2):c.532+28227T>C	rs2218279	0.51867
NM_012082.4(ZFPM2):c.1208C>G (p.Ala403Gly)	rs11993776	0.18341
NM_012082.4(ZFPM2):c.1362A>G (p.Pro454=)	rs920628	0.11991
NM_012082.4(ZFPM2):c.1776T>C (p.Pro592=)	rs16873732	0.05790
NM_012082.4(ZFPM2):c.1969A>G (p.Ser657Gly)	rs28374544	0.04474
NM_012082.4(ZFPM2):c.3369A>G (p.Leu1123=)	rs16873744	0.01580
NM_012082.4(ZFPM2):c.40+12C>G	rs149902904	0.00711
NM_012082.4(ZFPM2):c.292G>A (p.Asp98Asn)	rs202217256	0.00311
NM_012082.4(ZFPM2):c.1632G>A (p.Met544Ile)	rs187043152	0.00306
NM_012082.4(ZFPM2):c.533-4A>T	rs138466839	0.00296
NM_012082.4(ZFPM2):c.89A>G (p.Glu30Gly)	rs121908601	0.00293
NM_012082.4(ZFPM2):c.1276G>A (p.Ala426Thr)	rs35843564	0.00290
NM_012082.4(ZFPM2):c.629G>C (p.Ser210Thr)	rs182216711	0.00279
NM_012082.4(ZFPM2):c.739+19G>A	rs140283741	0.00160
NM_012082.4(ZFPM2):c.41-4C>A	rs374926066	0.00091
NM_012082.4(ZFPM2):c.1569G>C (p.Leu523=)	rs920629	0.00079
NM_012082.4(ZFPM2):c.1578G>T (p.Arg526=)	rs200643137	0.00066
NM_012082.4(ZFPM2):c.258A>G (p.Lys86=)	rs200972094	0.00025
NM_012082.4(ZFPM2):c.200-8T>G	rs573002259	0.00023
NM_012082.4(ZFPM2):c.2107A>C (p.Met703Leu)	rs121908603	0.00019
NM_012082.4(ZFPM2):c.1015G>A (p.Val339Ile)	rs201845067	0.00014
NM_012082.4(ZFPM2):c.1003C>G (p.Leu335Val)	rs376235097	0.00009
NM_012082.4(ZFPM2):c.1612G>A (p.Val538Ile)	rs575054307	0.00003
NM_012082.4(ZFPM2):c.421-5T>C	rs552410913	0.00003
NM_012082.4(ZFPM2):c.1255G>A (p.Glu419Lys)	rs374581095
NM_012082.4(ZFPM2):c.1770G>C (p.Lys590Asn)	rs533177469
NM_012082.4(ZFPM2):c.1818_1820del (p.Leu607del)	rs763555819
NM_012082.4(ZFPM2):c.191G>A (p.Cys64Tyr)
NM_012082.4(ZFPM2):c.2097C>T (p.His699=)	rs139368368
NM_012082.4(ZFPM2):c.3393T>G (p.Leu1131=)
NM_012082.4(ZFPM2):c.41-10C>G
NM_012082.4(ZFPM2):c.965-11T>C	rs189501457
NM_012082.4(ZFPM2):c.965-9TC[2]	rs147661076

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.