List of variants in gene combination ABCA12, SNHG31 reported by PreventionGenetics, part of Exact Sciences

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_173076.3(ABCA12):c.7105-17C>T	rs2274412	0.52421
NM_173076.3(ABCA12):c.6306C>T (p.Tyr2102=)	rs10498027	0.40571
NM_173076.3(ABCA12):c.7093G>A (p.Asp2365Asn)	rs726070	0.02339
NM_173076.3(ABCA12):c.5925C>T (p.Asp1975=)	rs6740406	0.01647
NM_173076.3(ABCA12):c.6501C>T (p.Asp2167=)	rs143387234	0.00655
NM_173076.3(ABCA12):c.6648G>T (p.Arg2216Ser)	rs145031776	0.00581
NM_173076.3(ABCA12):c.6208G>A (p.Val2070Ile)	rs145980660	0.00171
NM_173076.3(ABCA12):c.7631C>T (p.Thr2544Ile)	rs146834697	0.00143
NM_173076.3(ABCA12):c.6919A>G (p.Ile2307Val)	rs150196545	0.00105
NM_173076.3(ABCA12):c.6118-6C>T
NM_173076.3(ABCA12):c.6564A>C (p.Ala2188=)
NM_173076.3(ABCA12):c.6690A>G (p.Thr2230=)
NM_173076.3(ABCA12):c.6934G>C (p.Gly2312Arg)
NM_173076.3(ABCA12):c.7134C>T (p.His2378=)
NM_173076.3(ABCA12):c.7333A>G (p.Thr2445Ala)
NM_173076.3(ABCA12):c.7404A>G (p.Gln2468=)

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