Variant (rsID / SNP)

rs150974506

rs150974506 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIGG. Location: chromosome 4, position 509,983. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PIGGBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:509983
Cytoband: 4p16.3
HGVS: NM_001127178.3(PIGG):c.1114+9A>G
Allele change: Silent

Associated conditions / phenotypes

Intellectual disability, autosomal recessive 53

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.