ClinVar Miner

List of variants reported as likely benign for gingival disorder by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_002029.4(FPR1):c.607A>G (p.Ile203Val) rs150239733 0.00230
NM_002029.4(FPR1):c.26C>T (p.Thr9Met) rs148095693 0.00215
NM_002029.4(FPR1):c.368G>A (p.Arg123His) rs149931707 0.00041
NM_002029.4(FPR1):c.858A>G (p.Thr286=) rs371692364 0.00017
NM_002029.4(FPR1):c.553A>G (p.Asn185Asp) rs145973159 0.00016
NM_002029.4(FPR1):c.84C>T (p.Ile28=) rs143690932 0.00016
NM_002029.4(FPR1):c.1044G>A (p.Gln348=) rs150820622 0.00014
NM_002029.4(FPR1):c.744A>C (p.Ala248=) rs145578657 0.00013
NM_002029.4(FPR1):c.132C>T (p.Asn44=) rs762415254 0.00011
NM_002029.4(FPR1):c.414C>T (p.Thr138=) rs151277630 0.00010
NM_002029.4(FPR1):c.639C>T (p.Pro213=) rs141229910 0.00009
NM_002029.4(FPR1):c.957T>C (p.Ser319=) rs375541232 0.00008
NM_002029.4(FPR1):c.378C>T (p.Cys126=) rs776424230 0.00007
NM_002029.4(FPR1):c.582C>T (p.Ala194=) rs747540806 0.00007
NM_002029.4(FPR1):c.330C>T (p.Phe110=) rs539229723 0.00006
NM_002029.4(FPR1):c.564A>G (p.Lys188=) rs369805689 0.00006
NM_002029.4(FPR1):c.519A>T (p.Thr173=) rs748615602 0.00005
NM_002029.4(FPR1):c.189T>C (p.Ser63=) rs148014099 0.00004
NM_002029.4(FPR1):c.381C>T (p.Val127=) rs760563008 0.00004
NM_002029.4(FPR1):c.555C>T (p.Asn185=) rs539893573 0.00004
NM_002029.4(FPR1):c.738C>T (p.Val246=) rs148898220 0.00003
NM_002029.4(FPR1):c.942C>T (p.His314=) rs749154560 0.00003
NM_002029.4(FPR1):c.472T>C (p.Leu158=) rs1471159412 0.00002
NM_002029.4(FPR1):c.513G>A (p.Thr171=) rs554681504 0.00002
NM_002029.4(FPR1):c.543G>A (p.Ser181=) rs753325158 0.00002
NM_002029.4(FPR1):c.954C>G (p.Ala318=) rs766700447 0.00002
NM_002029.4(FPR1):c.156A>T (p.Gly52=) rs1389132373 0.00001
NM_002029.4(FPR1):c.21C>G (p.Leu7=) rs895586771 0.00001
NM_002029.4(FPR1):c.27G>A (p.Thr9=) rs771642804 0.00001
NM_002029.4(FPR1):c.300C>T (p.Phe100=) rs199764870 0.00001
NM_002029.4(FPR1):c.339C>A (p.Val113=) rs778269740 0.00001
NM_002029.4(FPR1):c.42G>A (p.Gly14=) rs866728748 0.00001
NM_002029.4(FPR1):c.474G>A (p.Leu158=) rs753449716 0.00001
NM_002029.4(FPR1):c.528C>T (p.Cys176=) rs769223294 0.00001
NM_002029.4(FPR1):c.1008C>A (p.Thr336=)
NM_002029.4(FPR1):c.1008C>T (p.Thr336=)
NM_002029.4(FPR1):c.12T>C (p.Asn4=) rs1479199724
NM_002029.4(FPR1):c.144C>T (p.Ile48=)
NM_002029.4(FPR1):c.15C>T (p.Ser5=)
NM_002029.4(FPR1):c.17C>T (p.Ser6Phe)
NM_002029.4(FPR1):c.204C>T (p.Ala68=) rs143480239
NM_002029.4(FPR1):c.258C>T (p.Ala86=)
NM_002029.4(FPR1):c.279C>T (p.Phe93=)
NM_002029.4(FPR1):c.27G>C (p.Thr9=) rs771642804
NM_002029.4(FPR1):c.30C>T (p.Asn10=) rs371185306
NM_002029.4(FPR1):c.333A>G (p.Gly111=)
NM_002029.4(FPR1):c.390A>G (p.Pro130=) rs2122323286
NM_002029.4(FPR1):c.405C>T (p.Asn135=)
NM_002029.4(FPR1):c.408C>T (p.His136=)
NM_002029.4(FPR1):c.439A>T (p.Ile147Phe) rs183314714
NM_002029.4(FPR1):c.444G>T (p.Gly148=)
NM_002029.4(FPR1):c.447C>T (p.Pro149=) rs778341723
NM_002029.4(FPR1):c.453G>A (p.Val151=) rs2122322988
NM_002029.4(FPR1):c.465C>T (p.Leu155=)
NM_002029.4(FPR1):c.486T>C (p.Ile162=) rs1848258347
NM_002029.4(FPR1):c.618C>T (p.Phe206=) rs2122322070
NM_002029.4(FPR1):c.624T>C (p.Ile208=)
NM_002029.4(FPR1):c.648C>T (p.Ile216=)
NM_002029.4(FPR1):c.696C>G (p.Gly232=)
NM_002029.4(FPR1):c.69C>T (p.Leu23=)
NM_002029.4(FPR1):c.705G>A (p.Lys235=) rs1599806461
NM_002029.4(FPR1):c.723G>T (p.Arg241=)
NM_002029.4(FPR1):c.726C>A (p.Val242=)
NM_002029.4(FPR1):c.726C>T (p.Val242=) rs143583727
NM_002029.4(FPR1):c.876C>T (p.Phe292=)
NM_002029.4(FPR1):c.918G>A (p.Gln306=)
NM_002029.4(FPR1):c.934C>T (p.Leu312=) rs2083741372
NM_002029.4(FPR1):c.960G>A (p.Leu320=)
NM_002029.4(FPR1):c.969C>T (p.Ala323=) rs2122320667
NM_002029.4(FPR1):c.975C>G (p.Thr325=) rs768152901

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