List of variants in gene TMEM67 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_153704.6(TMEM67):c.1645C>T (p.Arg549Cys)	rs747025617	0.00003
NM_153704.6(TMEM67):c.1038G>T (p.Trp346Cys)	rs754370463
NM_153704.6(TMEM67):c.2661+3A>G	rs568703831
NM_153704.6(TMEM67):c.2935G>A (p.Gly979Arg)
NM_153704.6(TMEM67):c.527C>T (p.Thr176Ile)

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