ClinVar Miner

List of variants in gene S1PR2 reported as likely benign by Labcorp Genetics (formerly Invitae), Labcorp

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_004230.4(S1PR2):c.923C>T (p.Pro308Leu) rs200973983 0.00049
NM_004230.4(S1PR2):c.179G>A (p.Arg60Gln) rs3745268 0.00017
NM_004230.4(S1PR2):c.570T>C (p.Tyr190=) rs142570783 0.00015
NM_004230.4(S1PR2):c.456C>T (p.Ile152=) rs539019136 0.00012
NM_004230.4(S1PR2):c.729C>T (p.Ile243=) rs148315102 0.00010
NM_004230.4(S1PR2):c.558C>T (p.Tyr186=) rs199954220 0.00009
NM_004230.4(S1PR2):c.981A>G (p.Pro327=) rs146709827 0.00008
NM_004230.4(S1PR2):c.901C>T (p.Arg301Trp) rs551166280 0.00005
NM_004230.4(S1PR2):c.1026G>A (p.Thr342=) rs377376944 0.00003
NM_004230.4(S1PR2):c.465G>A (p.Ser155=) rs571515815 0.00003
NM_004230.4(S1PR2):c.411C>T (p.Val137=) rs147860417 0.00002
NM_004230.4(S1PR2):c.615C>T (p.Ile205=) rs200948899 0.00002
NM_004230.4(S1PR2):c.90G>A (p.Thr30=) rs776010598 0.00002
NM_004230.4(S1PR2):c.228C>T (p.Ala76=) rs201361490 0.00001
NM_004230.4(S1PR2):c.258C>T (p.Phe86=) rs141451923 0.00001
NM_004230.4(S1PR2):c.297G>A (p.Arg99=) rs761534939 0.00001
NM_004230.4(S1PR2):c.393C>T (p.His131=) rs554534393 0.00001
NM_004230.4(S1PR2):c.486C>T (p.Leu162=) rs375693128 0.00001
NM_004230.4(S1PR2):c.81G>A (p.Thr27=) rs747435736 0.00001
NM_004230.4(S1PR2):c.963G>A (p.Pro321=) rs748108934 0.00001
NM_004230.4(S1PR2):c.999C>T (p.Ser333=) rs764691626 0.00001
NM_004230.4(S1PR2):c.198G>A (p.Ser66=) rs2039619619
NM_004230.4(S1PR2):c.216G>C (p.Leu72=)
NM_004230.4(S1PR2):c.303G>A (p.Thr101=)
NM_004230.4(S1PR2):c.370C>T (p.Leu124=)
NM_004230.4(S1PR2):c.378C>T (p.Ile126=)
NM_004230.4(S1PR2):c.426C>T (p.Ser142=)
NM_004230.4(S1PR2):c.429C>T (p.Asp143=) rs774990809
NM_004230.4(S1PR2):c.702G>A (p.Thr234=) rs1568275240
NM_004230.4(S1PR2):c.744C>A (p.Pro248=) rs141379245
NM_004230.4(S1PR2):c.780C>G (p.Pro260=)
NM_004230.4(S1PR2):c.783C>T (p.Val261=)
NM_004230.4(S1PR2):c.867G>A (p.Thr289=)
NM_004230.4(S1PR2):c.906G>A (p.Pro302=)
NM_004230.4(S1PR2):c.919A>T (p.Arg307Trp) rs2116942
NM_004230.4(S1PR2):c.993C>T (p.Ser331=) rs1381036491

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