List of variants in gene TUBB reported as uncertain significance for multiple benign circumferential skin creases on limbs 1

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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)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_178014.4(TUBB):c.161C>T (p.Ala54Val)	rs1776362492
NM_178014.4(TUBB):c.244G>C (p.Gly82Arg)	rs1776397001
NM_178014.4(TUBB):c.361C>T (p.Arg121Trp)	rs772730239
NM_178014.4(TUBB):c.801G>T (p.Met267Ile)

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