List of variants in gene IGF2, INS-IGF2 studied for chromosomal disorder

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000612.6(IGF2):c.466C>T (p.Arg156Cys)	rs1243657106	0.00001
NM_000612.6(IGF2):c.-6-2A>G
NM_000612.6(IGF2):c.-6-2A>T
NM_000612.6(IGF2):c.100G>T (p.Gly34Cys)	rs1858937359
NM_000612.6(IGF2):c.101G>A (p.Gly34Asp)	rs1858937182
NM_000612.6(IGF2):c.106del (p.Glu36fs)
NM_000612.6(IGF2):c.110_117delinsAGGTAA (p.Leu37fs)	rs1858936079
NM_000612.6(IGF2):c.157+1_157+2insGC	rs1114167321
NM_000612.6(IGF2):c.157+3A>C	rs1858932834
NM_000612.6(IGF2):c.195del (p.Ile66fs)	rs1858779370
NM_000612.6(IGF2):c.199G>A (p.Val67Ile)	rs1564894953
NM_000612.6(IGF2):c.1A>G (p.Met1Val)
NM_000612.6(IGF2):c.23C>A (p.Ser8Ter)	rs869320620
NM_000612.6(IGF2):c.243_244del (p.Glu81fs)
NM_000612.6(IGF2):c.252T>G (p.Cys84Trp)
NM_000612.6(IGF2):c.27del (p.Met9fs)	rs1858943428
NM_000612.6(IGF2):c.357G>A (p.Trp119Ter)
NM_000612.6(IGF2):c.59C>A (p.Ser20Ter)	rs142012621
NM_000612.6(IGF2):c.78C>G (p.Tyr26Ter)	rs1064794050

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