ClinVar Miner

List of variants in gene RAB27A reported as likely benign for albinism

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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NM_183235.3(RAB27A):c.*1392A>C rs12907749
NM_183235.3(RAB27A):c.*2067C>G rs7168226
NM_183235.3(RAB27A):c.*2349A>G rs76970799
NM_183235.3(RAB27A):c.*387A>G rs73407873
NM_183235.3(RAB27A):c.*731G>T rs76097718
NM_183235.3(RAB27A):c.*842G>A rs59982153
NM_183235.3(RAB27A):c.-142-5A>G rs61436564
NM_183235.3(RAB27A):c.195C>G (p.Gly65=) rs897453247

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