ClinVar for Gene (Select 23028) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3233507	NM_001009999.3(KDM1A):c.884-15A>G	KDM1A	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3113698	NM_001009999.3(KDM1A):c.659T>C (p.Ile220Thr)	KDM1A (I200T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3113697	NM_001009999.3(KDM1A):c.205T>C (p.Ser69Pro)	KDM1A (S69P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3068203	NM_001009999.3(KDM1A):c.711+1G>A	KDM1A	Single nucleotide variant (splice donor variant)	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome	GUncertain significance
Select item 3061086	NM_001009999.3(KDM1A):c.1486del (p.Arg496fs)	KDM1A (R472fs +2 more)	Deletion (frameshift variant)	KDM1A-related condition	GUncertain significance
Select item 3049013	NM_001009999.3(KDM1A):c.*9C>A	KDM1A	Single nucleotide variant (3 prime UTR variant)	KDM1A-related condition	GLikely benign
Select item 3047713	NM_001009999.3(KDM1A):c.352-6A>G	KDM1A	Single nucleotide variant (intron variant)	KDM1A-related condition	GLikely benign
Select item 3041271	NM_001009999.3(KDM1A):c.480T>A (p.Pro160=)	KDM1A	Single nucleotide variant (synonymous variant)	KDM1A-related condition	GLikely benign
Select item 3026778	NM_001009999.3(KDM1A):c.257G>T (p.Gly86Val)	KDM1A (G86V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3026416	NM_001009999.3(KDM1A):c.1434A>C (p.Lys478Asn)	KDM1A (K454N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3026120	NM_001009999.3(KDM1A):c.840T>A (p.Gly280=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024262	NM_001009999.3(KDM1A):c.1747G>C (p.Glu583Gln)	KDM1A (E559Q +3 more)	Single nucleotide variant (missense variant)	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome	GUncertain significance
Select item 3019356	NM_001009999.3(KDM1A):c.1031A>G (p.Asn344Ser)	KDM1A (N324S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3017278	NM_001009999.3(KDM1A):c.578-6C>T	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3010263	NM_001009999.3(KDM1A):c.578-5G>A	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2999422	NM_001009999.3(KDM1A):c.1414-6T>C	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2998962	NM_001009999.3(KDM1A):c.2025C>A (p.Val675=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989397	NM_001009999.3(KDM1A):c.1611G>A (p.Ala537=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2910100	NM_001009999.3(KDM1A):c.2028A>C (p.Gln676His)	KDM1A (Q676H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2908232	NM_001009999.3(KDM1A):c.712-5T>C	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2907017	NM_001009999.3(KDM1A):c.1635C>T (p.Leu545=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2902824	NM_001009999.3(KDM1A):c.1926C>T (p.Cys642=)	KDM1A	Single nucleotide variant (synonymous variant)	KDM1A-related condition +1 more	GLikely benign
Select item 2898841	NM_001009999.3(KDM1A):c.2538G>A (p.Ala846=)	KDM1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2898116	NM_001009999.3(KDM1A):c.2062T>G (p.Leu688Val)	KDM1A (L688V +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2896736	NM_001009999.3(KDM1A):c.1062A>T (p.Val354=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2894611	NM_001009999.3(KDM1A):c.1734+8T>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2891128	NM_001009999.3(KDM1A):c.2628G>A (p.Met876Ile)	KDM1A (M878I +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2881093	NM_001009999.3(KDM1A):c.1979C>T (p.Ala660Val)	KDM1A (A662V +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2879939	NM_001009999.3(KDM1A):c.1392A>G (p.Glu464=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2879513	NM_001009999.3(KDM1A):c.195T>A (p.Pro65=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878954	NM_001009999.3(KDM1A):c.256G>A (p.Gly86Ser)	KDM1A (G86S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2877003	NM_001009999.3(KDM1A):c.194C>G (p.Pro65Arg)	KDM1A (P65R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2876311	NM_001009999.3(KDM1A):c.975A>G (p.Thr325=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2875692	NM_001009999.3(KDM1A):c.2445+19A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2874973	NM_001009999.3(KDM1A):c.1893C>T (p.Thr631=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2874839	NM_001009999.3(KDM1A):c.2388C>T (p.Asp796=)	KDM1A	Single nucleotide variant (synonymous variant)	KDM1A-related condition +1 more	GLikely benign
Select item 2874738	NM_001009999.3(KDM1A):c.790+17A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2874685	NM_001009999.3(KDM1A):c.2627T>C (p.Met876Thr)	KDM1A (M852T +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2874019	NM_001009999.3(KDM1A):c.813A>T (p.Arg271=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2873749	NM_001009999.3(KDM1A):c.206C>T (p.Ser69Leu)	KDM1A (S69L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2873640	NM_001009999.3(KDM1A):c.2445+9C>A	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2871998	NM_001009999.3(KDM1A):c.351+18C>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2870975	NM_001009999.3(KDM1A):c.2310T>C (p.Thr770=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2870540	NM_001009999.3(KDM1A):c.2142G>C (p.Glu714Asp)	KDM1A (E714D +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2870435	NM_001009999.3(KDM1A):c.1414-17G>T	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2870429	NM_001009999.3(KDM1A):c.1072+11A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869832	NM_001009999.3(KDM1A):c.1167+12A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869684	NM_001009999.3(KDM1A):c.1542A>G (p.Leu514=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869656	NM_001009999.3(KDM1A):c.791-11T>C	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869150	NM_001009999.3(KDM1A):c.336G>T (p.Arg112=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868989	NM_001009999.3(KDM1A):c.21G>A (p.Ala7=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868066	NM_001009999.3(KDM1A):c.1179+18T>C	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867562	NM_001009999.3(KDM1A):c.2358C>G (p.Ser786=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867249	NM_001009999.3(KDM1A):c.196C>T (p.Pro66Ser)	KDM1A (P66S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2863210	NM_001009999.3(KDM1A):c.1288G>A (p.Val430Met)	KDM1A (V406M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2862584	NM_001009999.3(KDM1A):c.711+16A>T	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2862583	NM_001009999.3(KDM1A):c.711+15_711+16insGAAA	KDM1A	Insertion (intron variant)	not provided	GLikely benign
Select item 2861893	NM_001009999.3(KDM1A):c.2056-15T>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2860842	NM_001009999.3(KDM1A):c.1656dup (p.Leu553fs)	KDM1A (L553fs +3 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2860589	NM_001009999.3(KDM1A):c.1622+18A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2858961	NM_001009999.3(KDM1A):c.498T>G (p.Ser166Arg)	KDM1A (S166R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2853958	NM_001009999.3(KDM1A):c.987C>T (p.Ala329=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2845810	NM_001009999.3(KDM1A):c.1931C>T (p.Ala644Val)	KDM1A (A626V +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2841278	NM_001009999.3(KDM1A):c.540C>T (p.Asp180=)	KDM1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2837395	NM_001009999.3(KDM1A):c.1260_1295del (p.Asp421_Leu432del)	KDM1A	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2832654	NM_001009999.3(KDM1A):c.1218T>A (p.Phe406Leu)	KDM1A (F382L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2832594	NM_001009999.3(KDM1A):c.2486G>C (p.Arg829Pro)	KDM1A (R811P +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2830569	NM_001009999.3(KDM1A):c.290T>C (p.Met97Thr)	KDM1A (M97T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2829648	NM_001009999.3(KDM1A):c.2490C>T (p.Asn830=)	KDM1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2828853	NM_001009999.3(KDM1A):c.517+7T>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2824085	NM_001009999.3(KDM1A):c.352-13G>A	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2823958	NM_001009999.3(KDM1A):c.2106C>T (p.Phe702=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2821569	NM_001009999.3(KDM1A):c.203C>T (p.Ala68Val)	KDM1A (A68V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2821175	NM_001009999.3(KDM1A):c.1302G>A (p.Gln434=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2821090	NM_001009999.3(KDM1A):c.1861G>A (p.Ala621Thr)	KDM1A (A603T +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2818100	NM_001009999.3(KDM1A):c.368T>C (p.Met123Thr)	KDM1A (M123T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2813480	NM_001009999.3(KDM1A):c.885T>C (p.Thr295=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2809251	NM_001009999.3(KDM1A):c.1268A>G (p.Asn423Ser)	KDM1A (N399S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808870	NM_001009999.3(KDM1A):c.1161A>G (p.Gly387=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2807291	NM_001009999.3(KDM1A):c.2321G>A (p.Arg774His)	KDM1A (R750H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2805023	NM_001009999.3(KDM1A):c.990+16T>C	KDM1A	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2804312	NM_001009999.3(KDM1A):c.1168-19C>T	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2803909	NM_001009999.3(KDM1A):c.2056-7A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2803856	NM_001009999.3(KDM1A):c.2561T>G (p.Leu854Trp)	KDM1A (L854W +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2797503	NM_001009999.3(KDM1A):c.35C>T (p.Ala12Val)	KDM1A (A12V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2796668	NM_001009999.3(KDM1A):c.1497T>C (p.Thr499=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2795045	NM_001009999.3(KDM1A):c.790+18T>C	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2793111	NM_001009999.3(KDM1A):c.1158C>T (p.Asn386=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2792090	NM_001009999.3(KDM1A):c.899A>G (p.Lys300Arg)	KDM1A (K300R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2791745	NM_001009999.3(KDM1A):c.798T>C (p.Thr266=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2789156	NM_001009999.3(KDM1A):c.1191G>A (p.Glu397=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2786585	NM_001009999.3(KDM1A):c.696C>A (p.Phe232Leu)	KDM1A (F212L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2786540	NM_001009999.3(KDM1A):c.286C>T (p.Pro96Ser)	KDM1A (P96S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2785429	NM_001009999.3(KDM1A):c.2055+17A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2785428	NM_001009999.3(KDM1A):c.144C>G (p.Ala48=)	KDM1A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2784540	NM_001009999.3(KDM1A):c.1868-9C>T	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2784036	NM_001009999.3(KDM1A):c.161C>T (p.Ala54Val)	KDM1A (A54V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2783997	NM_001009999.3(KDM1A):c.352-4A>G	KDM1A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2783565	NM_001009999.3(KDM1A):c.31G>T (p.Ala11Ser)	KDM1A (A11S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2783401	NM_001009999.3(KDM1A):c.209C>T (p.Pro70Leu)	KDM1A (P70L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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