List of variants in gene RELN reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 46

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HGVS	dbSNP	gnomAD frequency
NM_005045.4(RELN):c.3712A>C (p.Asn1238His)	rs114003896	0.00468
NM_005045.4(RELN):c.4408G>A (p.Val1470Ile)	rs143213152	0.00232
NM_005045.4(RELN):c.77C>T (p.Ala26Val)	rs144557847	0.00154
NM_005045.4(RELN):c.3477C>A (p.Asn1159Lys)	rs114684479	0.00140
NM_005045.4(RELN):c.7181-19A>G	rs187689137	0.00127
NM_005045.4(RELN):c.3123C>T (p.Gly1041=)	rs41276148	0.00123
NM_005045.4(RELN):c.5880A>G (p.Thr1960=)	rs362793	0.00105
NM_005045.4(RELN):c.6141C>T (p.Phe2047=)	rs79161241	0.00098
NM_005045.4(RELN):c.1001G>A (p.Arg334His)	rs146922726	0.00091
NM_005045.4(RELN):c.577+7G>T	rs188372756	0.00091
NM_005045.4(RELN):c.4182A>G (p.Ser1394=)	rs147496823	0.00080
NM_005045.4(RELN):c.3913-9T>C	rs372473867	0.00076
NM_005045.4(RELN):c.6962C>T (p.Thr2321Met)	rs116065504	0.00064
NM_005045.4(RELN):c.3147-4A>G	rs375230548	0.00056
NM_005045.4(RELN):c.877G>A (p.Asp293Asn)	rs200289289	0.00033
NM_005045.4(RELN):c.2868C>T (p.His956=)	rs362694	0.00026
NM_005045.4(RELN):c.4872A>G (p.Gln1624=)	rs149121159	0.00024
NM_005045.4(RELN):c.4260G>A (p.Gly1420=)	rs150518726	0.00019
NM_005045.4(RELN):c.6647G>A (p.Arg2216Gln)	rs200010849	0.00017
NM_005045.4(RELN):c.7860C>T (p.Pro2620=)	rs116838125	0.00013
NM_005045.4(RELN):c.2637C>T (p.Val879=)	rs544717229	0.00008
NM_005045.4(RELN):c.7181-45T>C	rs779075555	0.00007
NM_005045.4(RELN):c.975A>G (p.Gln325=)	rs147568145	0.00006
NM_005045.4(RELN):c.5220G>A (p.Arg1740=)	rs774453752	0.00005
NM_005045.4(RELN):c.6735C>T (p.Pro2245=)	rs1158442529	0.00003
NM_005045.4(RELN):c.2703-9C>G	rs775212341	0.00001
NM_005045.4(RELN):c.4934T>C (p.Ile1645Thr)	rs537366000	0.00001
NM_005045.4(RELN):c.4936+7A>T	rs1219192080	0.00001
NM_005045.4(RELN):c.7938C>T (p.Asp2646=)	rs748558740	0.00001
NM_005045.4(RELN):c.-24GGC[11] (p.Met1_Glu2insGlyGlyGly)	rs55656324
NM_005045.4(RELN):c.-24GGC[15] (p.Met1_Glu2insGlyGlyGlyGlyGlyGlyGly)	rs55656324
NM_005045.4(RELN):c.-24GGC[6]	rs55656324
NM_005045.4(RELN):c.2208T>C (p.Phe736=)
NM_005045.4(RELN):c.3333+4T>G
NM_005045.4(RELN):c.3621G>A (p.Glu1207=)
NM_005045.4(RELN):c.4485G>T (p.Thr1495=)	rs542018962
NM_005045.4(RELN):c.5211-25_5211-24insG
NM_005045.4(RELN):c.5211-26G>T
NM_005045.4(RELN):c.5655C>T (p.Ser1885=)	rs558373106
NM_005045.4(RELN):c.5688T>C (p.Asp1896=)
NM_005045.4(RELN):c.6126A>G (p.Glu2042=)
NM_005045.4(RELN):c.6523+43_6523+44insTACATTG	rs745454190
NM_005045.4(RELN):c.6671+30dup	rs150971291
NM_005045.4(RELN):c.7181-24C>A
NM_005045.4(RELN):c.7181-24C>T
NM_005045.4(RELN):c.7181-28del

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