List of variants in gene MSH6 reported by OMIM

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_000179.3(MSH6):c.10C>T (p.Gln4Ter)	rs786201042	0.00002
NM_000179.3(MSH6):c.651dup (p.Lys218Ter)	rs63750955	0.00001
L222*
MSH6, 1-BP DEL, 594T
MSH6, 4-BP DEL, NT3609
NG_007111.1:g.2007_15002del
NM_000179.3(MSH6):c.1574_3439-428dup
NM_000179.3(MSH6):c.1596dup (p.Glu533Ter)	rs587779217
NM_000179.3(MSH6):c.1602del (p.Tyr535fs)	rs63751234
NM_000179.3(MSH6):c.3020G>A (p.Trp1007Ter)	rs587779252
NM_000179.3(MSH6):c.3053_3054del (p.Leu1018fs)	rs63751407
NM_000179.3(MSH6):c.3261del (p.Phe1088fs)	rs267608078
NM_000179.3(MSH6):c.3311_3312del (p.Phe1104fs)	rs267608092
NM_000179.3(MSH6):c.3386_3388del (p.Cys1129_Val1130delinsLeu)	rs587776705
NM_000179.3(MSH6):c.3633dup (p.Val1212fs)	rs587776706

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