ClinVar Miner

List of variants in gene AVPR2 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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NM_000054.6(AVPR2):c.*204C>T rs184401408
NM_000054.6(AVPR2):c.*257G>A rs73627263
NM_000054.6(AVPR2):c.1017G>A (p.Leu339=)
NM_000054.6(AVPR2):c.105G>A (p.Leu35=)
NM_000054.6(AVPR2):c.1113G>A (p.Ser371=) rs5203
NM_000054.6(AVPR2):c.117G>A (p.Ala39=)
NM_000054.6(AVPR2):c.125C>T (p.Ala42Val) rs5198
NM_000054.6(AVPR2):c.126G>A (p.Ala42=)
NM_000054.6(AVPR2):c.12G>A (p.Ala4=) rs61748993
NM_000054.6(AVPR2):c.174G>A (p.Val58=) rs201810684
NM_000054.6(AVPR2):c.19A>T (p.Thr7Ser) rs5196
NM_000054.6(AVPR2):c.26-6T>G rs56689668
NM_000054.6(AVPR2):c.311G>A (p.Arg104His)
NM_000054.6(AVPR2):c.317G>A (p.Arg106His)
NM_000054.6(AVPR2):c.35G>A (p.Gly12Glu) rs2071126
NM_000054.6(AVPR2):c.416G>A (p.Arg139His)
NM_000054.6(AVPR2):c.440C>T (p.Ala147Val) rs5200
NM_000054.6(AVPR2):c.546C>T (p.Asn182=)
NM_000054.6(AVPR2):c.643G>A (p.Val215Met) rs112109182
NM_000054.6(AVPR2):c.740G>A (p.Arg247His) rs149668713
NM_000054.6(AVPR2):c.742C>T (p.Arg248Cys)
NM_000054.6(AVPR2):c.769G>A (p.Gly257Ser)
NM_000054.6(AVPR2):c.927A>G (p.Leu309=) rs5201
NM_000054.6(AVPR2):c.993C>T (p.Ser331=) rs5202

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