ClinVar Miner

List of variants in gene GRIP1 reported as likely benign for Fraser syndrome 3

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001366722.1(GRIP1):c.2606G>A (p.Arg869Gln) rs145115262 0.00595
NM_001366722.1(GRIP1):c.*1314G>A rs144894732 0.00409
NM_001366722.1(GRIP1):c.2880G>A (p.Ser960=) rs181527317 0.00242
NM_001366722.1(GRIP1):c.2283G>A (p.Ser761=) rs200863167 0.00168
NM_001366722.1(GRIP1):c.2381T>G (p.Met794Arg) rs144494437 0.00155
NM_001366722.1(GRIP1):c.1645A>G (p.Ile549Val) rs201867922 0.00148
NM_001366722.1(GRIP1):c.160G>A (p.Val54Ile) rs199768740 0.00087
NM_001366722.1(GRIP1):c.2886G>A (p.Pro962=) rs375330927 0.00038
NM_001366722.1(GRIP1):c.1199-7C>G rs200313638 0.00029
NM_001366722.1(GRIP1):c.55+9C>A rs199740150 0.00025
NM_001366722.1(GRIP1):c.*234G>A rs541596282 0.00024
NM_001366722.1(GRIP1):c.579-8C>T rs375593950 0.00024
NM_001366722.1(GRIP1):c.1687+12T>C rs151041073 0.00023
NM_001366722.1(GRIP1):c.1688-3T>C rs185129168 0.00021
NM_001366722.1(GRIP1):c.1791A>G (p.Gly597=) rs768730046 0.00006
NM_001366722.1(GRIP1):c.162C>T (p.Val54=) rs759704197 0.00003
NM_001366722.1(GRIP1):c.1389G>A (p.Gly463=) rs200499586 0.00002
NM_001366722.1(GRIP1):c.*499A>G rs572566894 0.00001
NM_001366722.1(GRIP1):c.1787C>G (p.Pro596Arg) rs200955760
NM_001366722.1(GRIP1):c.418+14C>A rs79994510

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