List of variants in gene HNF1B reported as benign for Maturity onset diabetes mellitus in young

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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: 24

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.544+1391T>C	rs4430796	0.52088
NM_000458.4(HNF1B):c.1535-177T>C	rs2269841	0.34224
NM_000458.4(HNF1B):c.1535-225_1535-224insC	rs11440398	0.34179
NM_000458.4(HNF1B):c.1535-46T>G	rs2269842	0.29082
NM_000458.4(HNF1B):c.*384A>G	rs1058166	0.17933
NM_000458.4(HNF1B):c.1654-106C>T	rs8066605	0.08136
NM_000458.4(HNF1B):c.1534+252G>C	rs72830475	0.06206
NM_000458.4(HNF1B):c.344+228G>C	rs113656333	0.06093
NM_000458.4(HNF1B):c.345-228C>G	rs75979306	0.06037
NM_000458.4(HNF1B):c.345-19C>T	rs59527848	0.00765
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=)	rs140781855	0.00325
NM_000458.4(HNF1B):c.444G>A (p.Ser148=)	rs147218489	0.00228
NM_000458.4(HNF1B):c.1207-18T>C	rs199849203	0.00026
NM_000458.4(HNF1B):c.852C>T (p.His284=)	rs149581999	0.00022
NM_000458.4(HNF1B):c.*403A>G	rs557216745	0.00016
NM_000458.4(HNF1B):c.73G>T (p.Val25Leu)	rs139107479	0.00015
NM_000458.4(HNF1B):c.420C>T (p.Val140=)	rs370134885	0.00011
NM_000458.4(HNF1B):c.948C>T (p.Asp316=)	rs373132003	0.00006
NM_000458.4(HNF1B):c.1045+330G>T	rs9906451
NM_000458.4(HNF1B):c.1207-247_1207-246insGG	rs10701156
NM_000458.4(HNF1B):c.1207-7C>T	rs1215174368
NM_000458.4(HNF1B):c.135G>A (p.Thr45=)	rs2034121058
NM_000458.4(HNF1B):c.1488C>T (p.Ala496=)	rs773569563
NM_000458.4(HNF1B):c.477T>C (p.Pro159=)	rs1212716750

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