List of variants in gene SLC20A2, SMIM19 studied for hereditary dementia

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006749.4(SLC20A2):c.-534A>T	rs113755761	0.02320
NM_006749.4(SLC20A2):c.-592C>T	rs145711927	0.00840
NM_006749.4(SLC20A2):c.-457G>T	rs1206770675	0.00001
NM_006749.4(SLC20A2):c.-568C>A	rs1003849503	0.00001

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