"Ambry Genetics"[submitter] AND "G0S2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2483231	NM_015714.4(G0S2):c.16G>A (p.Glu6Lys)	G0S2, HSD11B1-AS1 (E6K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280314	NM_015714.4(G0S2):c.45G>A (p.Met15Ile)	G0S2, HSD11B1-AS1 (M15I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097717	NM_015714.4(G0S2):c.131A>T (p.Glu44Val)	G0S2, HSD11B1-AS1 (E44V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469708	NM_015714.4(G0S2):c.157G>A (p.Ala53Thr)	G0S2, HSD11B1-AS1 (A53T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364352	NM_015714.4(G0S2):c.174C>A (p.Asp58Glu)	G0S2, HSD11B1-AS1 (D58E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097719	NM_015714.4(G0S2):c.274G>A (p.Gly92Ser)	G0S2, HSD11B1-AS1 (G92S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343669	NM_015714.4(G0S2):c.277G>A (p.Gly93Ser)	G0S2, HSD11B1-AS1 (G93S)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar