List of variants in gene GSC studied for multiple congenital anomalies/dysmorphic syndrome

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_173849.3(GSC):c.108G>A (p.Pro36=)	rs191352872
NM_173849.3(GSC):c.196_212del (p.Gly66fs)	rs587777288
NM_173849.3(GSC):c.256G>C (p.Gly86Arg)	rs951684427
NM_173849.3(GSC):c.355+1G>C	rs587777290
NM_173849.3(GSC):c.400C>T (p.Gln134Ter)	rs587777289

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