Variant (rsID / SNP)

rs113994202

rs113994202 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAFAH1B1. Location: chromosome 17, position 2,575,939. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

PAFAH1B1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:2575939
Cytoband: 17p13.3
HGVS: NM_000430.4(PAFAH1B1):c.569-10T>C
Allele change: Silent

Associated conditions / phenotypes

Lissencephaly due to LIS1 mutation|Inborn genetic diseases|Lissencephaly

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.