"RHAG-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050561	NM_000324.3(RHAG):c.1139-8C>T	RHAG	Single nucleotide variant (intron variant)	RHAG-related condition	GLikely benign
Select item 2902956	NM_000324.3(RHAG):c.1057G>A (p.Ala353Thr)	RHAG (A353T)	Single nucleotide variant (missense variant)	RHAG-related condition +1 more	GLikely benign
Select item 2634109	NM_000324.3(RHAG):c.1018G>A (p.Val340Met)	RHAG (V340M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3035700	NM_000324.3(RHAG):c.808-10G>A	RHAG	Single nucleotide variant (intron variant)	RHAG-related condition	GLikely benign
Select item 2435420	NM_000324.3(RHAG):c.437T>C (p.Ile146Thr)	RHAG (I146T)	Single nucleotide variant (missense variant)	RHAG-related condition +1 more	GUncertain significance
Select item 2635235	NM_000324.3(RHAG):c.287T>C (p.Ile96Thr)	RHAG (I96T)	Single nucleotide variant (missense variant)	RHAG-related condition	GUncertain significance
Select item 1693914	NM_000324.3(RHAG):c.199T>C (p.Phe67Leu)	RHAG (F67L)	Single nucleotide variant (missense variant)	RHAG-related condition +1 more	GConflicting classifications of pathogenicity
Select item 13061	NM_000324.3(RHAG):c.157+1G>A	RHAG	Single nucleotide variant (splice donor variant)	RHAG-related condition	GPathogenic
Select item 2038181	NM_000324.3(RHAG):c.83C>T (p.Thr28Met)	RHAG (T28M)	Single nucleotide variant (missense variant)	RHAG-related condition +1 more	GLikely benign

ClinVar