List of variants in gene MSH2 reported by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.573C>T (p.Leu191=)	rs1800151	0.01972
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.1077-10T>C	rs17224360	0.01428
NM_000251.3(MSH2):c.2766T>C (p.Phe922=)	rs55859129	0.01118
NM_000251.3(MSH2):c.984C>T (p.Ala328=)	rs4987189	0.00495
NM_000251.3(MSH2):c.1666T>C (p.Leu556=)	rs61756466	0.00471
NM_000251.3(MSH2):c.339G>A (p.Lys113=)	rs35898375	0.00313
NM_000251.3(MSH2):c.23C>T (p.Thr8Met)	rs17217716	0.00184
NM_000251.3(MSH2):c.1277-8T>C	rs145400590	0.00159
NM_000251.3(MSH2):c.1387-8G>T	rs187525243	0.00143
NM_000251.3(MSH2):c.1737A>G (p.Lys579=)	rs61756467	0.00138
NM_000251.3(MSH2):c.1563T>C (p.Tyr521=)	rs63750330	0.00053
NM_000251.3(MSH2):c.815C>T (p.Ala272Val)	rs34136999	0.00046
NM_000251.3(MSH2):c.2154A>G (p.Gln718=)	rs63750810	0.00033
NM_000251.2(MSH2):c.-102T>C	rs17217709	0.00004
NM_000251.3(MSH2):c.964G>A (p.Gly322Ser)	rs773301485	0.00002
NM_000251.3(MSH2):c.10C>A (p.Gln4Lys)	rs878853797	0.00001
NM_000251.3(MSH2):c.2579C>T (p.Ser860Leu)	rs63750849	0.00001
NM_000251.3(MSH2):c.1032G>A (p.Gln344=)	rs375799148
NM_000251.3(MSH2):c.1276+10G>A	rs374061707
NM_000251.3(MSH2):c.2380A>C (p.Ile794Leu)	rs1553369778
NM_000251.3(MSH2):c.273TCT[2] (p.Leu94del)	rs267607919
NM_000251.3(MSH2):c.942+17_942+29del	rs11309117
NM_000251.3(MSH2):c.942+21_942+29del	rs11309117
NM_000251.3(MSH2):c.942+22_942+29del	rs11309117
NM_000251.3(MSH2):c.942+23_942+29del	rs11309117
NM_000251.3(MSH2):c.942+25_942+29del	rs11309117

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