SLC26A1[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1269605	NM_134425.4(SLC26A1):c.*158G>A	SLC26A1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1293883	NM_134425.4(SLC26A1):c.577-79C>T	SLC26A1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3359198	NM_022042.4(SLC26A1):c.514G>A (p.Gly172Arg)	SLC26A1 (G172R)	Single nucleotide variant (missense variant +1 more)	Nephrolithiasis susceptibility caused by SLC26A1	GLikely pathogenic

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