List of variants in gene PROM1 reported as likely benign for age-related macular degeneration

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_006017.3(PROM1):c.1345G>A (p.Val449Met)	rs200620291	0.00152
NM_006017.3(PROM1):c.2211+7C>T	rs372262346	0.00150
NM_006017.3(PROM1):c.714A>G (p.Gly238=)	rs201662148	0.00088
NM_006017.3(PROM1):c.1491G>T (p.Leu497Phe)	rs200520976	0.00070
NM_006017.3(PROM1):c.1928C>G (p.Ala643Gly)	rs62617075	0.00065
NM_006017.3(PROM1):c.2284A>G (p.Ser762Gly)	rs202029748	0.00058
NM_006017.3(PROM1):c.2112C>T (p.Arg704=)	rs375358457	0.00036
NM_006017.3(PROM1):c.1911+8G>A	rs370302107	0.00033
NM_006017.3(PROM1):c.963G>T (p.Leu321Phe)	rs202041422	0.00026
NM_006017.3(PROM1):c.2271C>T (p.Ile757=)	rs375986111	0.00022
NM_006017.3(PROM1):c.843C>T (p.His281=)	rs374394451	0.00019
NM_006017.3(PROM1):c.376G>A (p.Val126Met)	rs199556426	0.00009
NM_006017.3(PROM1):c.1152G>C (p.Arg384Ser)	rs201748228	0.00005
NM_006017.3(PROM1):c.2582+9A>C	rs200033458	0.00005
NM_006017.3(PROM1):c.1195C>T (p.Arg399Cys)	rs770268627	0.00004
NM_006017.3(PROM1):c.1199T>C (p.Leu400Pro)	rs140682455	0.00004
NM_006017.3(PROM1):c.1407G>A (p.Pro469=)	rs763710252	0.00004
NM_006017.3(PROM1):c.2364C>T (p.Ile788=)	rs551849678	0.00004
NM_006017.3(PROM1):c.1301+10T>A	rs192338518	0.00003
NM_006017.3(PROM1):c.1301+11C>A	rs189953160	0.00003
NM_006017.3(PROM1):c.276+15G>T	rs766012920	0.00003
NM_006017.3(PROM1):c.1377C>T (p.Gly459=)	rs779072238	0.00002
NM_006017.3(PROM1):c.1468A>T (p.Ser490Cys)	rs536622788	0.00002
NM_006017.3(PROM1):c.2578A>G (p.Thr860Ala)	rs747844753	0.00002
NM_006017.3(PROM1):c.1710C>T (p.Tyr570=)	rs201644238	0.00001
NM_006017.3(PROM1):c.1738A>C (p.Asn580His)	rs199674847	0.00001
NM_006017.3(PROM1):c.2309C>A (p.Pro770His)	rs568361529	0.00001
NM_006017.3(PROM1):c.158G>A (p.Gly53Asp)	rs755064227
NM_006017.3(PROM1):c.2094C>A (p.Ser698Arg)	rs199727800

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