List of variants reported as not provided for Microcephaly 7, primary, autosomal recessive

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001048166.1(STIL):c.257C>T (p.Ala86Val)	rs3125630	0.58260
NM_001048166.1(STIL):c.1136C>T (p.Ser379Phe)	rs149185431	0.00258
NM_001048166.1(STIL):c.3437C>T (p.Ala1146Val)	rs3766317	0.00007
NM_001048166.1(STIL):c.2957A>G (p.His986Arg)	rs199422205	0.00001
NM_001048166.1(STIL):c.1262A>C (p.Gln421Pro)	rs28472545
NM_001048166.1(STIL):c.1263A>C (p.Gln421His)	rs28705368
NM_001048166.1(STIL):c.2829+1G>A	rs199422206
NM_001048166.1(STIL):c.2858C>A (p.Ser953Tyr)	rs199422204
NM_001048166.1(STIL):c.3658del (p.Leu1219_Val1220insTer)	rs199422207
NM_001048166.1(STIL):c.3718C>T (p.Gln1240Ter)	rs121918609

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