List of variants in gene combination LOC129999735, MNX1 reported as uncertain significance for Currarino triad

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005515.4(MNX1):c.509C>G (p.Ala170Gly)	rs746725337	0.00006
NM_005515.4(MNX1):c.478G>A (p.Gly160Ser)
NM_005515.4(MNX1):c.504GGC[6] (p.Ala174dup)	rs748208450
NM_005515.4(MNX1):c.520G>T (p.Ala174Ser)

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