ClinVar Miner

List of variants in gene CRB2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_173689.7(CRB2):c.1600C>T (p.Arg534Trp) rs759002273
NM_173689.7(CRB2):c.1859G>C (p.Cys620Ser) rs879255250
NM_173689.7(CRB2):c.1882C>T (p.Arg628Cys) rs202128397
NM_173689.7(CRB2):c.1886G>C (p.Cys629Ser) rs879255252
NM_173689.7(CRB2):c.1897C>T (p.Arg633Trp) rs730880377
NM_173689.7(CRB2):c.1928A>C (p.Glu643Ala) rs730880300
NM_173689.7(CRB2):c.2277G>A (p.Trp759Ter) rs375072557
NM_173689.7(CRB2):c.2400C>G (p.Asn800Lys) rs765676223
NM_173689.7(CRB2):c.3089_3104dup (p.Gly1036fs) rs879255251
NM_173689.7(CRB2):c.3190C>T (p.Pro1064Ser) rs868484209
NM_173689.7(CRB2):c.3559A>C (p.Thr1187Pro) rs1554785663
NM_173689.7(CRB2):c.3746G>A (p.Arg1249Gln) rs147412276

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