List of variants in gene TMEM138 reported as benign for central nervous system malformation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_016464.5(TMEM138):c.261G>A (p.Val87=)	rs35245221	0.01861
NM_016464.5(TMEM138):c.-24G>A	rs116455434	0.00930
NM_016464.5(TMEM138):c.216C>T (p.Asn72=)	rs145939072	0.00035
NM_016464.5(TMEM138):c.327C>T (p.Ser109=)	rs201318247	0.00028
NM_016464.5(TMEM138):c.387G>A (p.Leu129=)	rs553815473	0.00004
NM_016464.5(TMEM138):c.129-11dup

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