ClinVar Miner

List of variants reported as likely benign for atrial fibrillation, familial, 11 by Invitae

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 68
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_181703.4(GJA5):c.995G>A (p.Arg332His) rs116551187 0.00037
NM_181703.4(GJA5):c.111G>A (p.Leu37=) rs138362351 0.00031
NM_181703.4(GJA5):c.13A>G (p.Ser5Gly) rs144069395 0.00025
NM_181703.4(GJA5):c.348G>A (p.Glu116=) rs150168016 0.00019
NM_181703.4(GJA5):c.798C>T (p.Asp266=) rs116155008 0.00014
NM_181703.4(GJA5):c.973A>C (p.Asn325His) rs782592443 0.00011
NM_181703.4(GJA5):c.864C>T (p.Ala288=) rs1384966203 0.00003
NM_181703.4(GJA5):c.342C>G (p.Ala114=) rs886045251 0.00002
NM_181703.4(GJA5):c.378G>A (p.Pro126=) rs112980895 0.00002
NM_181703.4(GJA5):c.867C>T (p.Ser289=) rs782795886 0.00002
NM_181703.4(GJA5):c.1065C>T (p.Asp355=) rs201657244 0.00001
NM_181703.4(GJA5):c.147G>A (p.Gln49=) rs1487739192 0.00001
NM_181703.4(GJA5):c.258C>T (p.Ser86=) rs782415947 0.00001
NM_181703.4(GJA5):c.516C>T (p.Tyr172=) rs369888327 0.00001
NM_181703.4(GJA5):c.1023G>A (p.Lys341=) rs145008952
NM_181703.4(GJA5):c.105C>T (p.Leu35=)
NM_181703.4(GJA5):c.1071A>T (p.Ser357=) rs1553226734
NM_181703.4(GJA5):c.117A>G (p.Thr39=) rs2148959468
NM_181703.4(GJA5):c.123T>A (p.Ala41=) rs2148959454
NM_181703.4(GJA5):c.138G>A (p.Gly46=) rs984101534
NM_181703.4(GJA5):c.138G>C (p.Gly46=)
NM_181703.4(GJA5):c.213C>T (p.Pro71=)
NM_181703.4(GJA5):c.255C>A (p.Val85=)
NM_181703.4(GJA5):c.261G>A (p.Thr87=)
NM_181703.4(GJA5):c.268C>T (p.Leu90=)
NM_181703.4(GJA5):c.297T>G (p.Thr99=) rs146738543
NM_181703.4(GJA5):c.30C>T (p.Phe10=)
NM_181703.4(GJA5):c.327G>A (p.Arg109=) rs143695986
NM_181703.4(GJA5):c.351C>T (p.Val117=)
NM_181703.4(GJA5):c.381G>A (p.Val127=)
NM_181703.4(GJA5):c.399G>T (p.Leu133=)
NM_181703.4(GJA5):c.414A>G (p.Glu138=)
NM_181703.4(GJA5):c.432C>A (p.Ala144=)
NM_181703.4(GJA5):c.435C>T (p.Leu145=)
NM_181703.4(GJA5):c.438G>A (p.Gln146=) rs1553226989
NM_181703.4(GJA5):c.445C>T (p.Leu149=)
NM_181703.4(GJA5):c.447G>C (p.Leu149=) rs782002899
NM_181703.4(GJA5):c.450C>T (p.Leu150=)
NM_181703.4(GJA5):c.510C>A (p.Gly170=)
NM_181703.4(GJA5):c.513G>A (p.Gln171=) rs1571066735
NM_181703.4(GJA5):c.525C>T (p.Tyr175=)
NM_181703.4(GJA5):c.537G>C (p.Leu179=) rs2148959118
NM_181703.4(GJA5):c.543C>T (p.Thr181=) rs1553226953
NM_181703.4(GJA5):c.544C>T (p.Leu182=) rs1553226951
NM_181703.4(GJA5):c.559A>C (p.Arg187=)
NM_181703.4(GJA5):c.567C>G (p.Pro189=) rs2148959089
NM_181703.4(GJA5):c.576C>T (p.His192=)
NM_181703.4(GJA5):c.57C>G (p.Thr19=)
NM_181703.4(GJA5):c.591C>T (p.Tyr197=)
NM_181703.4(GJA5):c.618C>G (p.Val206=) rs2148959048
NM_181703.4(GJA5):c.645T>A (p.Ala215=)
NM_181703.4(GJA5):c.685C>T (p.Leu229=)
NM_181703.4(GJA5):c.738T>C (p.Ala246=) rs2148958978
NM_181703.4(GJA5):c.756C>A (p.Gly252=)
NM_181703.4(GJA5):c.765G>C (p.Val255=) rs2148958937
NM_181703.4(GJA5):c.780C>T (p.Ser260=) rs1663834363
NM_181703.4(GJA5):c.789A>G (p.Pro263=)
NM_181703.4(GJA5):c.795C>T (p.Pro265=)
NM_181703.4(GJA5):c.813G>A (p.Leu271=) rs2148958892
NM_181703.4(GJA5):c.81T>C (p.Thr27=)
NM_181703.4(GJA5):c.843T>C (p.Asn281=)
NM_181703.4(GJA5):c.870A>G (p.Gln290=)
NM_181703.4(GJA5):c.891C>T (p.Val297=)
NM_181703.4(GJA5):c.903A>G (p.Val301=) rs2148958793
NM_181703.4(GJA5):c.945T>A (p.Val315=) rs2148958748
NM_181703.4(GJA5):c.948T>A (p.Arg316=)
NM_181703.4(GJA5):c.963T>G (p.Pro321=)
NM_181703.4(GJA5):c.978A>C (p.Gly326=)

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.