Related gene-specific medical variations for Gene (Select 285800) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3310447	NM_175922.4(PRR18):c.76C>T (p.Pro26Ser)	LOC129997654, PRR18 (P26S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219371	NM_175922.4(PRR18):c.257C>T (p.Ala86Val)	LOC129997654, PRR18 (A86V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219370	NM_175922.4(PRR18):c.250G>A (p.Ala84Thr)	LOC129997654, PRR18 (A84T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219369	NM_175922.4(PRR18):c.242C>G (p.Pro81Arg)	LOC129997654, PRR18 (P81R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612247	NM_175922.4(PRR18):c.251C>G (p.Ala84Gly)	LOC129997654, PRR18 (A84G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568975	NM_175922.4(PRR18):c.158T>C (p.Leu53Pro)	LOC129997654, PRR18 (L53P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551946	NM_175922.4(PRR18):c.211G>A (p.Ala71Thr)	LOC129997654, PRR18 (A71T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509611	NM_175922.4(PRR18):c.16A>T (p.Met6Leu)	LOC129997654, PRR18 (M6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390065	NM_175922.4(PRR18):c.91G>A (p.Asp31Asn)	LOC129997654, PRR18 (D31N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377579	NM_175922.4(PRR18):c.188G>T (p.Gly63Val)	LOC129997654, PRR18 (G63V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351736	NM_175922.4(PRR18):c.220G>A (p.Gly74Ser)	LOC129997654, PRR18 (G74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345851	NM_175922.4(PRR18):c.22C>T (p.Pro8Ser)	LOC129997654, PRR18 (P8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276943	NM_175922.4(PRR18):c.205C>A (p.Pro69Thr)	LOC129997654, PRR18 (P69T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238281	NM_175922.4(PRR18):c.26C>T (p.Pro9Leu)	LOC129997654, PRR18 (P9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance