List of variants in gene LAMA2 reported as uncertain significance by Athena Diagnostics Inc

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile)	rs112388307	0.00103
NM_000426.4(LAMA2):c.922G>A (p.Glu308Lys)	rs146462599	0.00086
NM_000426.4(LAMA2):c.1400A>G (p.Lys467Arg)	rs138162760	0.00071
NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr)	rs34505698	0.00066
NM_000426.4(LAMA2):c.5689G>A (p.Ala1897Thr)	rs200518204	0.00021
NM_000426.4(LAMA2):c.2325C>A (p.Asn775Lys)	rs139351727	0.00019
NM_000426.4(LAMA2):c.4909G>A (p.Glu1637Lys)	rs138303386	0.00019
NM_000426.4(LAMA2):c.7057C>T (p.Arg2353Cys)	rs145885540	0.00016
NM_000426.4(LAMA2):c.1873A>G (p.Ile625Val)	rs141658354	0.00014
NM_000426.4(LAMA2):c.3628A>G (p.Ile1210Val)	rs147291222	0.00014
NM_000426.4(LAMA2):c.4969G>A (p.Val1657Met)	rs370971334	0.00014
NM_000426.4(LAMA2):c.5291A>G (p.Glu1764Gly)	rs141950826	0.00014
NM_000426.4(LAMA2):c.8011C>A (p.Pro2671Thr)	rs780695627	0.00014
NM_000426.4(LAMA2):c.8147G>A (p.Arg2716His)	rs142781107	0.00011
NM_000426.4(LAMA2):c.4436+8T>C	rs192650285	0.00009
NM_000426.4(LAMA2):c.479A>T (p.Asp160Val)	rs147398243	0.00006
NM_000426.4(LAMA2):c.1550A>T (p.Glu517Val)	rs372358704	0.00005
NM_000426.4(LAMA2):c.5050G>A (p.Glu1684Lys)	rs201632009	0.00004
NM_000426.4(LAMA2):c.6539A>T (p.Asp2180Val)	rs567385461	0.00004
NM_000426.4(LAMA2):c.7118C>T (p.Ser2373Leu)	rs758887080	0.00004
NM_000426.4(LAMA2):c.9060G>A (p.Leu3020=)	rs368896579	0.00004
NM_000426.4(LAMA2):c.2477G>A (p.Arg826Gln)	rs759973830	0.00003
NM_000426.4(LAMA2):c.6518A>T (p.Asn2173Ile)	rs529110314	0.00003
NM_000426.4(LAMA2):c.1262C>A (p.Ser421Tyr)	rs775603569	0.00001
NM_000426.4(LAMA2):c.1681T>G (p.Leu561Val)	rs765515681	0.00001
NM_000426.4(LAMA2):c.2376C>T (p.Phe792=)	rs150046431	0.00001
NM_000426.4(LAMA2):c.2794A>G (p.Ser932Gly)	rs761539740	0.00001
NM_000426.4(LAMA2):c.488A>T (p.Tyr163Phe)	rs201175472	0.00001
NM_000426.4(LAMA2):c.5899G>T (p.Ala1967Ser)	rs762129616	0.00001
NM_000426.4(LAMA2):c.6079C>A (p.Pro2027Thr)	rs374006928	0.00001
NM_000426.4(LAMA2):c.6659C>T (p.Pro2220Leu)	rs367665458	0.00001
NM_000426.4(LAMA2):c.7346T>C (p.Ile2449Thr)	rs1156828795	0.00001
NM_000426.4(LAMA2):c.1623T>A (p.Ser541Arg)
NM_000426.4(LAMA2):c.2239G>T (p.Gly747Cys)
NM_000426.4(LAMA2):c.3317G>A (p.Cys1106Tyr)	rs371548755
NM_000426.4(LAMA2):c.4321C>A (p.His1441Asn)	rs1562477412
NM_000426.4(LAMA2):c.4909G>C (p.Glu1637Gln)	rs138303386
NM_000426.4(LAMA2):c.5284C>G (p.Arg1762Gly)	rs746492572
NM_000426.4(LAMA2):c.6332A>T (p.Asp2111Val)
NM_000426.4(LAMA2):c.6764T>C (p.Ile2255Thr)	rs951339046
NM_000426.4(LAMA2):c.6952T>A (p.Phe2318Ile)	rs757197871
NM_000426.4(LAMA2):c.8244+3_8244+6del	rs746678525
NM_000426.4(LAMA2):c.8857G>A (p.Val2953Ile)	rs1211031170

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