List of variants reported as uncertain significance for Seckel syndrome 1 by Genetic Services Laboratory,University of Chicago

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Total variants: 13

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HGVS	dbSNP
NM_001184.4(ATR):c.1350-3T>C	rs587783323
NM_001184.4(ATR):c.2290A>G (p.Lys764Glu)	rs77208665
NM_001184.4(ATR):c.2688G>A (p.Leu896=)	rs117926957
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly)	rs149008479
NM_001184.4(ATR):c.3799G>A (p.Val1267Ile)	rs377689383
NM_001184.4(ATR):c.4306A>G (p.Asn1436Asp)	rs587783328
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp)	rs148064542
NM_001184.4(ATR):c.4641+15C>T	rs200619976
NM_001184.4(ATR):c.5732A>G (p.Asn1911Ser)	rs587783334
NM_001184.4(ATR):c.5739-14G>T	rs587783335
NM_001184.4(ATR):c.6961T>C (p.Phe2321Leu)	rs587783338
NM_001184.4(ATR):c.7041+4G>C	rs113544835
NM_001184.4(ATR):c.7725G>A (p.Ala2575=)	rs587783340

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