Variant (rsID / SNP)

rs150318966

rs150318966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYGD. Location: chromosome 2, position 208,986,546. Clinical significance in the table: Benign.

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Reference-table entries

CRYGDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:208986546
Cytoband: 2q33.3
HGVS: NM_006891.4(CRYGD):c.376G>A (p.Val126Met)
Allele change: Silent

Associated conditions / phenotypes

Cataract 4 multiple types|Aculeiform cataract

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.