List of variants in gene PSAP reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002778.4(PSAP):c.1432-22C>T	rs885828	0.34727
NM_002778.4(PSAP):c.1005+18C>T	rs55829339	0.14035
NM_002778.4(PSAP):c.-4C>T	rs2070188	0.12811
NM_002778.4(PSAP):c.1006-21C>T	rs56214505	0.01471
NM_002778.4(PSAP):c.-10A>G	rs76455588	0.01197
NM_002778.4(PSAP):c.721-13T>C	rs370875535	0.00025
NM_002778.4(PSAP):c.1519G>C (p.Glu507Gln)	rs149000433	0.00021
NM_002778.4(PSAP):c.1172C>T (p.Thr391Met)	rs202125074	0.00010
NM_002778.4(PSAP):c.249+6C>T	rs774663731	0.00006
NM_002778.4(PSAP):c.154G>A (p.Val52Ile)	rs147920923	0.00003
NM_002778.4(PSAP):c.1350+4C>T	rs769353440	0.00001
NM_002778.4(PSAP):c.1137G>C (p.Glu379Asp)	rs754680319
NM_002778.4(PSAP):c.1193-26G>A	rs3747860
NM_002778.4(PSAP):c.717C>G (p.Asp239Glu)
NM_002778.4(PSAP):c.956A>G (p.Glu319Gly)

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