List of variants in gene MSH6 reported as likely pathogenic by Mendelics

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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_000179.3(MSH6):c.3226C>T (p.Arg1076Cys)	rs63750617	0.00002
NM_000179.3(MSH6):c.1634_1635del (p.Lys545fs)	rs267608064
NM_000179.3(MSH6):c.3018C>A (p.Tyr1006Ter)	rs1553414395
NM_000179.3(MSH6):c.3646G>C (p.Gly1216Arg)	rs1114167690
NM_000179.3(MSH6):c.3753_3756dup (p.Val1253fs)	rs876661222
NM_000179.3(MSH6):c.3996_3999dup (p.Arg1334fs)	rs1553333753

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