List of variants in gene SLC1A2 reported as benign for electroclinical syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004171.4(SLC1A2):c.731-8T>C	rs2273689	0.55092
NM_004171.4(SLC1A2):c.1221A>G (p.Val407=)	rs1042113	0.26392
NM_004171.4(SLC1A2):c.603G>A (p.Pro201=)	rs752949	0.22188
NM_004171.4(SLC1A2):c.562-36T>C	rs3895234	0.22153
NM_004171.4(SLC1A2):c.311-37A>G	rs10836370	0.20991
NM_004171.4(SLC1A2):c.157+31C>G	rs2273687	0.19605

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