"Ambry Genetics"[submitter] AND "LOC126862130"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3183418	NM_017672.6(TRPM7):c.4051T>C (p.Ser1351Pro)	LOC126862130, TRPM7 (S1351P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408141	NM_017672.6(TRPM7):c.4043C>G (p.Ala1348Gly)	LOC126862130, TRPM7 (A1348G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474469	NM_017672.6(TRPM7):c.3898T>C (p.Ser1300Pro)	LOC126862130, TRPM7 (S1300P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458569	NM_017672.6(TRPM7):c.3880G>A (p.Val1294Ile)	LOC126862130, TRPM7 (V1294I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183417	NM_017672.6(TRPM7):c.3808A>C (p.Ile1270Leu)	LOC126862130, TRPM7 (I1270L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244881	NM_017672.6(TRPM7):c.3656A>G (p.Asn1219Ser)	LOC126862130, TRPM7 (N1219S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329306	NM_017672.6(TRPM7):c.3650G>A (p.Arg1217His)	LOC126862130, TRPM7 (R1217H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar