"GeneDx"[submitter] AND "RHAG"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1221020	NM_000324.3(RHAG):c.1212+207C>A	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183810	NM_000324.3(RHAG):c.946-18T>C	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234058	NM_000324.3(RHAG):c.946-100T>C	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241378	NM_000324.3(RHAG):c.946-171C>T	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282036	NM_000324.3(RHAG):c.945+76del	RHAG	Deletion (intron variant)	not provided	GBenign
Select item 225454	NM_000324.3(RHAG):c.808G>A (p.Val270Ile)	RHAG (V270I)	Single nucleotide variant (missense variant)	Rh-null, regulator type +2 more	GBenign/Likely benign
Select item 1271298	NM_000324.3(RHAG):c.808-236A>G	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269541	NM_000324.3(RHAG):c.808-300A>G	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296822	NM_000324.3(RHAG):c.808-311T>C	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270189	NM_000324.3(RHAG):c.807+280C>T	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273508	NM_000324.3(RHAG):c.807+112G>A	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267811	NM_000324.3(RHAG):c.641-51G>A	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1297957	NM_000324.3(RHAG):c.341+260G>C	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229804	NM_000324.3(RHAG):c.158-152A>G	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228066	NM_000324.3(RHAG):c.158-267T>C	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179802	NM_000324.3(RHAG):c.158-298T>G	RHAG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253810	GRCh37/hg19 6p12.3(chr6:48682849-49834213)x3	RHAG, CENPQ +7 more	Copy number gain	See cases	GUncertain significance