ClinVar Miner

List of variants in gene GRHL2 reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_024915.4(GRHL2):c.*123C>T rs115933929 0.01551
NM_024915.4(GRHL2):c.21-24C>T rs73701923 0.01188
NM_024915.4(GRHL2):c.1099-189A>T rs116616762 0.01137
NM_024915.4(GRHL2):c.1764-139T>C rs74337254 0.01120
NM_024915.4(GRHL2):c.734+246C>A rs113751811 0.00678
NM_024915.4(GRHL2):c.1486-213T>C rs113897997 0.00656
NM_024915.4(GRHL2):c.1517+145G>C rs113141118 0.00606
NM_024915.4(GRHL2):c.1698+174T>A rs142905063 0.00558
NM_024915.4(GRHL2):c.1004-96G>A rs185375766 0.00501
NM_024915.4(GRHL2):c.1500G>A (p.Thr500=) rs34550163 0.00460
NM_024915.4(GRHL2):c.1345+124C>T rs148523911 0.00458
NM_024915.4(GRHL2):c.1517+12A>G rs142083150 0.00458
NM_024915.4(GRHL2):c.1517+119C>G rs146684067 0.00457
NM_024915.4(GRHL2):c.1517+35A>G rs115164415 0.00457
NM_024915.4(GRHL2):c.1517+66C>T rs191641315 0.00457
NM_024915.4(GRHL2):c.1485+173C>T rs115747617 0.00399
NM_024915.4(GRHL2):c.1098+9C>T rs189993760 0.00370
NM_024915.4(GRHL2):c.1764-41C>T rs116327133 0.00272
NM_024915.4(GRHL2):c.1098+42C>A rs75368465 0.00183
NM_024915.4(GRHL2):c.804C>T (p.Thr268=) rs55682875 0.00076
NM_024915.4(GRHL2):c.689G>A (p.Ser230Asn) rs140423160 0.00059
NM_024915.4(GRHL2):c.454G>A (p.Val152Met) rs147703146 0.00047
NM_024915.4(GRHL2):c.543G>A (p.Glu181=) rs200674096 0.00035
NM_024915.4(GRHL2):c.1698+7C>T rs199657203 0.00023
NM_024915.4(GRHL2):c.1098+6T>C rs776382416 0.00019
NM_024915.4(GRHL2):c.1763+29T>G rs372962065 0.00016
NM_024915.4(GRHL2):c.849C>T (p.Thr283=) rs138628340 0.00011
NM_024915.4(GRHL2):c.1416T>C (p.Pro472=) rs371708806 0.00010
NM_024915.4(GRHL2):c.1641C>T (p.Asp547=) rs759288104 0.00008
NM_024915.4(GRHL2):c.1863G>A (p.Thr621=) rs201588336 0.00008
NM_024915.4(GRHL2):c.303T>A (p.Ser101Arg) rs140106332 0.00008
NM_024915.4(GRHL2):c.816A>G (p.Lys272=) rs760857170 0.00007
NM_024915.4(GRHL2):c.1245C>T (p.Val415=) rs779878869 0.00005
NM_024915.4(GRHL2):c.1836G>A (p.Glu612=) rs201346001 0.00005
NM_024915.4(GRHL2):c.981G>A (p.Ala327=) rs368774126 0.00004
NM_024915.4(GRHL2):c.*28G>A rs188265528 0.00003
NM_024915.4(GRHL2):c.987G>A (p.Gln329=) rs200745936 0.00003
NM_024915.4(GRHL2):c.1029G>A (p.Thr343=) rs767022758 0.00002
NM_024915.4(GRHL2):c.678+7C>T rs780311020 0.00002
NM_024915.4(GRHL2):c.1095G>A (p.Ala365=) rs267601683 0.00001
NM_024915.4(GRHL2):c.1152G>A (p.Val384=) rs776545912 0.00001
NM_024915.4(GRHL2):c.1763+18C>G rs758362384 0.00001
NM_024915.4(GRHL2):c.417C>T (p.Tyr139=) rs768143303 0.00001
NM_024915.4(GRHL2):c.1003+12T>C
NM_024915.4(GRHL2):c.1029G>T (p.Thr343=)
NM_024915.4(GRHL2):c.1080C>T (p.Asp360=)
NM_024915.4(GRHL2):c.1099-15T>C
NM_024915.4(GRHL2):c.1116T>C (p.Asn372=)
NM_024915.4(GRHL2):c.1299C>T (p.Asn433=)
NM_024915.4(GRHL2):c.1345+16A>C
NM_024915.4(GRHL2):c.1485+8C>T
NM_024915.4(GRHL2):c.1486-172AC[25] rs3029438
NM_024915.4(GRHL2):c.1517+17T>C
NM_024915.4(GRHL2):c.1517+8A>T
NM_024915.4(GRHL2):c.1613-20C>G
NM_024915.4(GRHL2):c.1613-20C>T
NM_024915.4(GRHL2):c.1698+18T>C
NM_024915.4(GRHL2):c.1722C>T (p.Pro574=)
NM_024915.4(GRHL2):c.1764-12C>A
NM_024915.4(GRHL2):c.1764-12C>G rs371424751
NM_024915.4(GRHL2):c.1764-16C>T
NM_024915.4(GRHL2):c.1764-40G>A rs375774210
NM_024915.4(GRHL2):c.1806G>A (p.Ser602=) rs61732855
NM_024915.4(GRHL2):c.1809C>T (p.Asn603=)
NM_024915.4(GRHL2):c.183T>G (p.Ala61=)
NM_024915.4(GRHL2):c.192C>T (p.Leu64=)
NM_024915.4(GRHL2):c.20+15C>G
NM_024915.4(GRHL2):c.20+17C>T
NM_024915.4(GRHL2):c.20+544G>C
NM_024915.4(GRHL2):c.21-4A>G
NM_024915.4(GRHL2):c.217-58T>C rs113798475
NM_024915.4(GRHL2):c.284+19C>G
NM_024915.4(GRHL2):c.669A>G (p.Ala223=)
NM_024915.4(GRHL2):c.678+8C>T
NM_024915.4(GRHL2):c.679-18A>T
NM_024915.4(GRHL2):c.679-20C>T
NM_024915.4(GRHL2):c.679-4G>T
NM_024915.4(GRHL2):c.734+8A>T
NM_024915.4(GRHL2):c.753C>T (p.Thr251=)
NM_024915.4(GRHL2):c.81A>G (p.Arg27=)
NM_024915.4(GRHL2):c.87C>T (p.Tyr29=)
NM_024915.4(GRHL2):c.892-16A>G
NM_024915.4(GRHL2):c.892-18C>T

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