Variant (rsID / SNP)

rs150920905

rs150920905 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MKKS. Location: chromosome 20, position 10,394,147. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MKKSBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 20:10394147
Cytoband: 20p12.2
HGVS: NM_170784.3(MKKS):c.16G>A (p.Ala6Thr)
Allele change: Missense_A6T

Associated conditions / phenotypes

Bardet-Biedl syndrome|McKusick-Kaufman syndrome|Bardet-Biedl syndrome 6|McKusick-Kaufman syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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