ClinVar Miner

List of variants in gene ARL6 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Gene type:
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Total variants: 25
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HGVS dbSNP
GRCh38/hg38 3q11.2(chr3:97790061-97794169)
NM_001278293.3(ARL6):c.*225G>C rs4857294
NM_001278293.3(ARL6):c.*255C>T rs79196822
NM_001278293.3(ARL6):c.*284C>A rs148380165
NM_001278293.3(ARL6):c.*470G>A rs184213166
NM_001278293.3(ARL6):c.-137A>C rs192372191
NM_001278293.3(ARL6):c.-207G>A rs189005414
NM_001278293.3(ARL6):c.-71C>G rs777066573
NM_001278293.3(ARL6):c.140T>A (p.Ile47Asn)
NM_001278293.3(ARL6):c.185+1G>C rs1559679965
NM_001278293.3(ARL6):c.351_353delinsGAAAA (p.Asp117fs) rs1057515576
NM_001278293.3(ARL6):c.364C>T (p.Arg122Ter) rs104893678
NM_001278293.3(ARL6):c.480-8C>T rs77010939
NM_001278293.3(ARL6):c.506G>C (p.Gly169Ala) rs104893679
NM_001278293.3(ARL6):c.509T>G (p.Leu170Trp) rs104893681
NM_001278293.3(ARL6):c.536-4T>C rs201939836
NM_001278293.3(ARL6):c.92C>G (p.Thr31Arg) rs104893680
NM_001278293.3(ARL6):c.92C>T (p.Thr31Met) rs104893680
NM_032146.5(ARL6):c.*275G>A rs886058939
NM_032146.5(ARL6):c.-245T>C rs886058937
NM_032146.5(ARL6):c.-28+531A>T rs143739859
NM_032146.5(ARL6):c.-339C>T rs116162146
NM_032146.5(ARL6):c.272T>C (p.Ile91Thr) rs137854907
NM_032146.5(ARL6):c.350-13_350-2del
NM_032146.5(ARL6):c.526T>C (p.Trp176Arg) rs886058938

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