List of variants reported as likely benign for Nephrolithiasis, calcium oxalate by Fulgent Genetics, Fulgent Genetics

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_022042.4(SLC26A1):c.1115G>A (p.Arg372His)	rs73219719	0.01054
NM_022042.4(SLC26A1):c.1713C>G (p.Ala571=)	rs36069160	0.00995
NM_000203.5(IDUA):c.235G>A (p.Ala79Thr)	rs58037052	0.00910
NM_022042.4(SLC26A1):c.534C>T (p.Ile178=)	rs36095812	0.00611
NM_022042.4(SLC26A1):c.1043T>C (p.Leu348Pro)	rs148386572	0.00222
NM_022042.4(SLC26A1):c.1906G>T (p.Asp636Tyr)	rs146466185	0.00158
NM_022042.4(SLC26A1):c.1511G>A (p.Arg504His)	rs201106151	0.00150
NM_022042.4(SLC26A1):c.181C>T (p.Arg61Cys)	rs547128457	0.00084
NM_022042.4(SLC26A1):c.153G>C (p.Gln51His)	rs200471470	0.00028
NM_022042.4(SLC26A1):c.1296G>A (p.Pro432=)	rs150810594	0.00023
NM_022042.4(SLC26A1):c.432C>T (p.Ala144=)	rs143284684	0.00021
NM_022042.4(SLC26A1):c.1785G>A (p.Pro595=)	rs148200047	0.00016
NM_022042.4(SLC26A1):c.315C>G (p.Ser105=)	rs377636525	0.00014
NM_022042.4(SLC26A1):c.1152C>T (p.Asn384=)	rs140876735	0.00013
NM_022042.4(SLC26A1):c.1869C>T (p.Asp623=)	rs144567476	0.00011
NM_022042.4(SLC26A1):c.1116T>C (p.Arg372=)	rs559991759	0.00009
NM_022042.4(SLC26A1):c.1404G>A (p.Pro468=)	rs370491888	0.00009
NM_022042.4(SLC26A1):c.1848C>T (p.Cys616=)	rs377435206	0.00009
NM_022042.4(SLC26A1):c.1557G>A (p.Thr519=)	rs146711224	0.00004
NM_022042.4(SLC26A1):c.1854G>A (p.Pro618=)	rs748205966	0.00004
NM_022042.4(SLC26A1):c.654G>A (p.Gly218=)	rs375888392	0.00002
NM_022042.4(SLC26A1):c.1506C>T (p.Ala502=)	rs753883088	0.00001
NM_022042.4(SLC26A1):c.639T>C (p.Asp213=)	rs369163740	0.00001
NM_022042.4(SLC26A1):c.1686G>A (p.Thr562=)	rs199549367
NM_022042.4(SLC26A1):c.577-15G>A	rs192314032

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