ClinVar Miner

Variants in gene TMEM67 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 12
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HGVS dbSNP
NM_001142301.1(TMEM67):c.1045+46C>T rs73694952
NM_001142301.1(TMEM67):c.107C>T (p.Pro36Leu) rs73324992
NM_001142301.1(TMEM67):c.263+48G>A rs73694924
NM_001142301.1(TMEM67):c.264-19T>C rs138589757
NM_001142301.1(TMEM67):c.2665-43C>T rs56307046
NM_001142301.1(TMEM67):c.627-29A>G rs116802062
NM_001142301.1(TMEM67):c.823-3C>T rs3097427
NM_153704.6(TMEM67):c.1810A>G (p.Ile604Val) rs3134031
NM_153704.6(TMEM67):c.2161C>T (p.Pro721Ser) rs116445698
NM_153704.6(TMEM67):c.25G>A (p.Val9Met) rs199961375
NM_153704.6(TMEM67):c.2892A>C (p.Thr964=) rs16916221
NM_153704.6(TMEM67):c.781G>A (p.Asp261Asn) rs35793208

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