List of variants reported as pathogenic for Congenital short bowel syndrome, autosomal recessive by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_024769.5(CLMP):c.821G>A (p.Arg274Gln)	rs587776965	0.00001
NM_024769.5(CLMP):c.230del (p.Glu77fs)	rs587776964
NM_024769.5(CLMP):c.371T>A (p.Val124Asp)	rs587776967
NM_024769.5(CLMP):c.664C>T (p.Arg222Ter)	rs587776966

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