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Variant (rsID / SNP)

rs1191778

WDR35

rs1191778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR35. Location: chromosome 2, position 20,131,079. Clinical significance in the table: Benign.

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Reference-table entries

WDR35Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
2:20131079
Cytoband
2p24.1
HGVS
NM_020779.4(WDR35):c.2915A>G (p.Glu972Gly)
Allele change
Missense_E983G

Associated conditions / phenotypes

Short-rib thoracic dysplasia 7 with or without polydactyly|Cranioectodermal dysplasia 2|Short-rib thoracic dysplasia 7 with or without polydactyly|Cranioectodermal dysplasia 2

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.